Disposal of Hazardous Waste in Underground Mines (Sustainable World)

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Disposal of Hazardous Waste in Underground Mines

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The Sustainable World Aims and Objectives Sustainability is a key concept of 21st century planning in that it broadly determines the ability of the current generation to use resources and live a lifestyle without compromising the ability of future generations to do the same. Sustainability affects our environment, economics, security, resources, health, economics, transport and information decisions strategy. It also encompasses decision making, from the highest administrative office, to the basic community level. It is planned that this Book Series will cover many of these aspects across a range of topical fields for the greater appreciation and understanding of all those involved in researching or implementing sustainability projects in their field of work.

Topics Data Analysis Data Mining Methodologies Risk Management Brownfield Development Landscaping and Visual Impact Studies Public Health Issues Environmental and Urban Monitoring Waste Management Energy Use and Conservation Institutional, Legal and Economic Issues Education Visual Impact

Simulation Systems Forecasting Infrastructure and Maintenance Mobility and Accessibility Strategy and Development Studies Environment Pollution and Control Land Use Transport, Traffic and Integration City, Urban and Industrial Planning The Community and Urban Living Public Safety and Security Global Trends

Main Editor

E. Tiezzi University of Siena Italy

Associate Editors

D. Almorza University of Cadiz Spain

D. Emmanouloudis Technical Educational Institute of Kavala Greece

M. Andretta Montecatini Italy

J.W. Everett Rowan University USA

A. Bejan Duke University USA

R.J. Fuchs United Nations Chile

A. Bogen Down to Earth USA

F. Gomez Universidad Politecnica de Valencia Spain

I. Cruzado University of Puerto Rico-Mayazuez Puerto Rico

K.G. Goulias Pennsylvania State University USA

W. Czyczula Krakow University of Technology Poland

A.H. Hendrickx Free University of Brussels Belgium

M. Davis Temple University USA

I. Hideaki Nagoya University Japan

K. Dorow Pacific Northwest National Laboratory USA

S.E. Jørgensen The University of Pharmeceutical Science Denmark

C. Dowlen South Bank University UK

D. Kaliampakos National Technical University of Athens Greece

H. Kawashima The University of Tokyo Japan

J. Park Seoul National University Korea

B.A. Kazimee Washington State University USA

M.F. Platzer Naval Postgraduate School USA

D. Kirkland Nicholas Grimshaw & Partners UK

V. Popov Wessex Institute of Technology UK

A. Lebedev Moscow State University USA

A.D. Rey McGill University Canada

D. Lewis Mississippi State Univesity USA

H. Sozer Illinois Institute of Technology USA

N. Marchettini University of Siena Italy

A. Teodosio Pontificia Univ. Catolica de Minas Gerais Brazil

J.F. Martin-Duque Universidad Complutense Spain

W. Timmermans Green World Research The Netherlands

M.B. Neace Mercer University USA

R. van Duin Delft University of Technology The Netherlands

R. Olsen Camp Dresser & McKee Inc. USA

G. Walters University of Exeter UK

M.S. Palo The Finnish Forestry Research Institute Finland


Disposal of Hazardous Waste in Underground Mines Editors V. Popov Wessex Institute of Technology, UK R. Pusch GeoDevelopment AB, Sweden

Disposal of Hazardous Waste in Underground Mines Series: The Sustainable World, Volume 11 Editors V. Popov Wessex Institute of Technology, UK

R. Pusch GeoDevelopment AB, Sweden

Published by WIT Press Ashurst Lodge, Ashurst, Southampton, SO40 7AA, UK Tel: 44 (0) 238 029 3223; Fax: 44 (0) 238 029 2853 E-Mail: [email protected] http://www.witpress.com For USA, Canada and Mexico WIT Press 25 Bridge Street, Billerica, MA 01821, USA Tel: 978 667 5841; Fax: 978 667 7582 E-Mail: [email protected] http://www.witpress.com British Library Cataloguing-in-Publication Data A Catalogue record for this book is available from the British Library ISBN: 1-85312-750-7 ISSN: 1476-9581 Library of Congress Catalog Card Number: 2006921658 No responsibility is assumed by the Publisher, the Editors and Authors for any injury and/or damage to persons or property as a matter of products liability, negligence or otherwise, or from any use or operation of any methods, products, instructions or ideas contained in the material herein. © WIT Press 2006 Printed in Great Britain by Athenaeum Press Ltd., Gateshead. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without the prior written permission of the Publisher.

Contents

Preface: Towards a safer future Chapter 1 Hazardous waste generation and management in Europe ................................ D. Kaliampakos, A. Mavropoulos & M. Menegaki 1.1 1.2 1.3 1.4

1.5 1.6

1.7

Introduction ............................................................................................. Hazardous waste generation in Europe ................................................... 1.2.1 Hazardous waste generation per employee ................................ 1.2.2 Main waste streams in Europe .................................................... Current hazardous waste management in Europe ................................... Trends and expectations .......................................................................... 1.4.1 Dangerous substances from waste streams and EU priorities................................................................................ 1.4.2 Future trends up to 2010 ............................................................. 1.4.3 Emission trends of heavy metals ................................................ 1.4.4 Emission trends of pesticides and POPs..................................... The effect of Directive 99/31 .................................................................. Waste streams and pollutants of interest ................................................. 1.6.1 Waste streams of interest ............................................................ 1.6.2 Pollutants of interest ................................................................... 1.6.3 Selection of the pollutants of interest ......................................... 1.6.4 Chemical substances ................................................................... 1.6.4.1 Chemicals of concern.................................................. 1.6.5 Heavy metals............................................................................... 1.6.5.1 Heavy metals in water pathways................................. 1.6.5.2 Heavy metals in soil.................................................... 1.6.5.3 Heavy metals in food .................................................. 1.6.6 Persistent organic pollutants ....................................................... 1.6.6.1 Polycyclic aromatic hydrocarbons.............................. 1.6.6.2 Organochlorines dispersal in soil, groundwater and some global-scale problems ................................. Conclusions .............................................................................................

xvii 1 1 2 4 5 7 9 9 14 14 15 16 17 17 18 18 19 22 22 22 23 23 23 23 24 27

Chapter 2 Need and potential for underground disposal – survey of underground mines in Europe ................................................................................................ 33 D. Kaliampakos, A. Mavropoulos & M. Menegaki 2.1 2.2 2.3

2.4

Surface vs. underground hazardous waste disposal facilities................................................................................................... Survey of underground mines in Europe ................................................ The profile of mining activity in 15 EU countries .................................. 2.3.1 Austria ...................................................................................... 2.3.2 Belgium .................................................................................... 2.3.3 Denmark ................................................................................... 2.3.4 Finland...................................................................................... 2.3.5 France ....................................................................................... 2.3.6 Germany ................................................................................... 2.3.7 Greece....................................................................................... 2.3.8 Ireland....................................................................................... 2.3.9 Italy........................................................................................... 2.3.10 Luxembourg ............................................................................. 2.3.11 Portugal .................................................................................... 2.3.12 Spain......................................................................................... 2.3.13 Sweden ..................................................................................... 2.3.14 The Netherlands ....................................................................... 2.3.15 The United Kingdom................................................................ Inactive underground mines used as waste disposal sites....................... 2.4.1 Morsleben salt mine ................................................................. 2.4.2 Herfa-Neurode salt mine .......................................................... 2.4.3 Konrad iron mine...................................................................... 2.4.4 Stripa iron mine ........................................................................ 2.4.5 Asse salt mine...........................................................................

33 34 38 38 39 39 40 40 41 41 42 43 44 44 45 46 48 48 50 50 52 55 57 58

Chapter 3 Criteria for selecting repository mines ............................................................. 61 R. Pusch 3.1 3.2

3.3

Introduction............................................................................................. Rock structure ......................................................................................... 3.2.1 Crystalline rock ........................................................................ 3.2.2 Argillaceous rock ..................................................................... 3.2.3 Salt rock.................................................................................... 3.2.4 Other rock types ....................................................................... Requirements for the use of mines as repositories.................................. 3.3.1 Function of the host rock.......................................................... 3.3.2 Conversion of mines to repositories......................................... 3.3.3 Size ........................................................................................... 3.3.4 Remaining exploitable ore........................................................

61 62 62 62 65 67 67 67 67 68 68

3.3.5

3.4

Rock structure, hydrology, and stability..................................... 3.3.5.1 General ........................................................................ 3.3.5.2 Rock structure modelling ............................................ 3.3.6 Transport to and in the mine....................................................... 3.3.7 Facilities and installations........................................................... 3.3.8 Stabilization ................................................................................ 3.3.9 Cost ............................................................................................. Reference mines ...................................................................................... 3.4.1 General........................................................................................ 3.4.2 Crystalline rock........................................................................... 3.4.2.1 The Stripa Mine .......................................................... 3.4.2.2 Regional rock structure ............................................... 3.4.2.3 Local rock structure .................................................... 3.4.2.4 Rooms ......................................................................... 3.4.2.5 Rock stress conditions................................................. 3.4.2.6 Rock stability issues.................................................... 3.4.2.7 Hydrology in the far-field and near-field .................... 3.4.3 Salt and argillaceous rock ...........................................................

68 68 69 70 71 71 71 72 72 72 72 72 73 74 75 76 77 77

Chapter 4 Engineered barriers ........................................................................................... 79 R. Pusch 4.1

4.2

4.3

4.4

Types and characteristics of engineered barriers .................................... 4.1.1 Clay ............................................................................................. 4.1.1.1 Fundamental behaviour of clay/water systems ........... 4.1.1.2 Clay materials for waste isolation............................... Methods for constructing engineered barriers in underground mines .................................................................................. 4.2.1 Materials ..................................................................................... 4.2.2 Preparation and application of smectite clay barriers................. 4.2.2.1 Compaction of blocks ................................................. 4.2.2.2 Layerwise application and compaction....................... Maturation of smectite clay barriers........................................................ 4.3.1 Background ................................................................................. 4.3.2 Clay microstructure..................................................................... 4.3.3 Hydration .................................................................................... 4.3.3.1 Mechanisms ................................................................ 4.3.3.2 Rate of hydration......................................................... The source term ....................................................................................... 4.4.1 Definitions................................................................................... 4.4.2 Tests ............................................................................................ 4.4.2.1 Alkaline batteries in Friedland Ton ............................ 4.4.2.2 Chemical interaction of clay and corroded batteries .......................................................................

80 80 80 82 88 88 88 89 90 92 92 92 93 93 94 99 99 99 99 101

4.4.2.3

4.5

4.6

4.7

Chemical interaction of clay and uncorroded Hg batteries ................................................................. 4.4.2.4 Other hazardous waste ................................................ Basis for modelling transport of hazardous elements from the waste .................................................................................................. 4.5.1 General........................................................................................ 4.5.1.1 Definition of the source term ...................................... 4.5.2 Safety aspects.............................................................................. Long-term chemical stability of smectite................................................ 4.6.1 General........................................................................................ 4.6.2 Conversion of smectite to non-expandable minerals (‘illitization’) .............................................................................. 4.6.3 Chemical interaction of smectite clay and cement ..................... Cost estimates.......................................................................................... 4.7.1 Disposal of batteries (mixed with clay powder and compacted to blocks) ................................................................. 4.7.2 Disposal of solidified pesticides (sandwiched clay and clay/waste layers) .......................................................................

102 102 103 103 103 105 106 106 106 107 111 111 112

Chapter 5 Stability analysis of mines ................................................................................ 115 R. Adey & A. Calaon 5.1 5.2

5.3

5.4 5.5

5.6

Background and objective of the work ................................................... 5.1.1 Concept model for prediction ..................................................... 5.1.2 Mine disposal concept ................................................................ Modelling methodology .......................................................................... 5.2.1 Mohr–Coulomb criterion ............................................................ 5.2.2 EDZ divided in subzones............................................................ 5.2.3 Submodelling .............................................................................. 5.2.4 Some experiments to determine the required model details....... Description of cases to be studied and modelling assumptions .............. 5.3.1 Limestone – room and pillar....................................................... 5.3.2 Crystalline rock........................................................................... 5.3.2.1 Global (outer) model................................................... 5.3.2.2 Submodel .................................................................... Material properties................................................................................... Results of stability analysis ..................................................................... 5.5.1 Case of mine in limestone........................................................... 5.5.1.1 Case 1: Centre of the mine.......................................... 5.5.1.2 Case 2: On the edge of the mine ................................. 5.5.2 Crystalline rock........................................................................... 5.5.2.1 Case 3: Global model.................................................. 5.5.2.2 Submodel .................................................................... Conclusions .............................................................................................

116 116 116 117 118 119 119 120 125 125 129 130 133 134 135 135 135 137 141 141 143 151

Chapter 6 Risk assessment of underground repositories using numerical modelling of flow and transport in fractured rock ............................................ 157 V. Popov & A. Peratta 6.1

6.2

6.3

6.4 6.5

Overview of the problem......................................................................... 6.1.1 Scope and objectives................................................................... 6.1.2 Fractured porous media .............................................................. 6.1.3 Overview..................................................................................... 6.1.3.1 The continuum approach............................................. 6.1.3.2 The very near field zone.............................................. 6.1.3.3 The near field flow ...................................................... 6.1.3.4 The far field model ...................................................... 6.1.3.5 The very far field model.............................................. 6.1.3.6 The discrete fracture model......................................... 6.1.4 Historical development of porous media modelling .................. Governing equations................................................................................ 6.2.1 Flow ............................................................................................ 6.2.1.1 General formulation .................................................... 6.2.1.2 Flow in the porous matrix ........................................... 6.2.1.3 Flow in a single fracture.............................................. 6.2.1.4 Fracture intersections .................................................. 6.2.1.5 Flow in pipe connectors .............................................. 6.2.2 Transport ..................................................................................... 6.2.2.1 General formulation .................................................... 6.2.2.2 Transport in the porous matrix.................................... 6.2.2.3 Transport in a single fracture ...................................... 6.2.2.4 Transport in pipes........................................................ 6.2.2.5 Transport in pipe connectors....................................... Numerical method ................................................................................... 6.3.1 Introduction................................................................................. 6.3.2 The boundary element method ................................................... 6.3.2.1 Integral formulation .................................................... 6.3.2.2 Boundary discretization .............................................. 6.3.2.3 Internal solution .......................................................... 6.3.3 The dual reciprocity method ....................................................... 6.3.3.1 General approach ........................................................ 6.3.3.2 Radial basis functions ................................................. 6.3.3.3 The reaction term ........................................................ 6.3.3.4 The convective term.................................................... 6.3.3.5 Time integration scheme............................................. 6.3.3.6 Domain decomposition and DRM–MD...................... Computational implementation ............................................................... Results ..................................................................................................... 6.5.1 Types of geological media considered .......................................

158 158 159 159 159 159 159 160 160 160 161 162 162 162 163 163 164 165 165 166 167 167 167 168 168 168 168 168 170 172 172 173 174 175 175 176 176 178 180 181

6.5.2

The waste types considered ........................................................ 6.5.2.1 Dichlorvos ................................................................... 6.5.2.2 Zinc ............................................................................. 6.5.3 Case of mine and tunnel in crystalline rock ............................... 6.5.3.1 Geometry definition .................................................... 6.5.3.2 Model discretization.................................................... 6.5.3.3 Parameter estimation................................................... 6.5.3.4 Boundary and initial conditions .................................. 6.5.3.5 Results for flow ........................................................... 6.5.4 Case of disposal of dichlorvos in mine repository in crystalline rock............................................................................ 6.5.4.1 Modelling conditions for dichlorvos........................... 6.5.4.2 Transport results for dichlorvos .................................. 6.5.5 Case of disposal of zinc in mine repository in crystalline rock............................................................................ 6.5.5.1 Modelling conditions for zinc..................................... 6.5.5.2 Transport results for zinc ............................................ 6.5.6 Case of mine in limestone........................................................... 6.5.6.1 Geometry definition .................................................... 6.5.6.2 Parameter estimation................................................... 6.5.6.3 Boundary and initial conditions .................................. 6.5.6.4 Results for flow ........................................................... 6.5.7 Case of disposal of dichlorvos in mine repository in limestone ..................................................................................... 6.5.7.1 Modelling conditions for dichlorvos........................... 6.5.7.2 Transport results for dichlorvos .................................. 6.5.8 Case of disposal of zinc in mine repository in limestone........... 6.5.8.1 Modelling conditions for zinc..................................... 6.5.8.2 Transport results for zinc ............................................ Risk assessment summary .......................................................................

199 199 200 206 206 206 207

Appendix to Chapter 2 A2.1 Austria .................................................................................................. A2.1.1 Active mines and mineral production................................... A2.1.2 Inactive mines ....................................................................... A2.2 Belgium ................................................................................................ A2.2.1 Active mines and mineral production................................... A2.2.2 Inactive mines ....................................................................... A2.3 Denmark ............................................................................................... A2.3.1 Active mines and mineral production................................... A2.3.2 Inactive mines ....................................................................... A2.4 Finland .................................................................................................. A2.4.1 Active mines and mineral production................................... A2.4.2 Inactive mines .......................................................................

213 213 214 214 214 215 216 216 217 217 217 223

6.6

181 181 182 182 182 184 185 185 187 189 189 190 196 196 197 197 198 198 198 198

A2.5 A2.6 A2.7 A2.8 A2.9 A2.10 A2.11 A2.12 A2.13 A2.14 A2.15

Index

France ................................................................................................. A2.5.1 Active mines and mineral production............................... A2.5.2 Inactive mines ................................................................... Germany ............................................................................................. A2.6.1 Active mines and mineral production............................... A2.6.2 Inactive mines ................................................................... Greece................................................................................................. A2.7.1 Active mines and mineral production............................... A2.7.2 Inactive mines ................................................................... Ireland................................................................................................. A2.8.1 Active mines and mineral production............................... A2.8.2 Inactive mines ................................................................... Italy..................................................................................................... A2.9.1 Active mines and mineral production............................... A2.9.2 Inactive mines ................................................................... Luxembourg ....................................................................................... A2.10.1 Mines and mineral production .......................................... Portugal............................................................................................... A2.11.1 Active mines and mineral production............................... A2.11.2 Inactive mines ................................................................... Spain ................................................................................................... A2.12.1 Active mines and mineral production............................... A2.12.2 Inactive mines ................................................................... Sweden ............................................................................................... A2.13.1 Active mines and mineral production............................... A2.13.2 Inactive mines ................................................................... The Netherlands.................................................................................. A2.14.1 Active mines and mineral production............................... A2.14.2 Inactive mines ................................................................... The United Kingdom.......................................................................... A2.15.1 Active mines and mineral production............................... A2.15.2 Inactive mines ...................................................................

223 223 225 226 226 227 230 230 233 235 235 236 236 236 239 240 240 240 240 244 244 244 248 250 250 253 256 256 256 256 256 258 259


Preface: Towards a safer future

This book summarizes the ideas and concepts of a group of European business and academic centres from UK, Sweden, Germany and Greece on disposal of hazardous waste (HW) in underground mines. This collaboration started as a result of a joint multidisciplinary European effort sponsored by the European Commission as part of the Energy, Environment and Sustainable Development Programme under the project title Low Risk Disposal Technology (LowRiskDT). The developed theoretical concepts and practical application technologies were further advanced by the group since the conclusion of the LowRiskDT Project, and the main findings of this joint work are summarized in this book. The research work was focused on: the possibility of using abandoned underground mines for disposal of hazardous chemical waste with negligible pollution of the environment; the properties and behaviour of waste-isolating clay materials and practical ways of preparing and applying them; development of software tools to assess the stability, performance and risks associated with different repository concepts, considering the long-term safety of the biosphere; the isolating capacity of reference repositories; and the different approaches for handling hazardous chemical waste. The project has demonstrated that HW can be safely disposed in underground mines provided that adequate assessment, planning and design procedures are employed. Abandoned mines are sites where advanced exploration or mining activities ceased without rehabilitation having been implemented at all or completed. There are many abandoned mines in the EU where environmental and economic benefits would exist if those mines are used for disposal of HW. Disposal of HW in abandoned underground mines would in many cases reduce environmental risks from pollution after sealing the mine workings. Industry and waste management companies will benefit from this alternative approach by gaining access to a safe and relatively cheap strategy for dealing with HW. Since the assessment of suitable mines must be done on a case-by-case basis, this book cannot specify a certain type of mine as suitable for safe disposal of HW. However, research has led to the definition of the interdisciplinary scientific approach needed to identify the suitable mine types, and also the technology needed in order to achieve safe disposal of HW in underground mines. The results

of a comparison between underground storage of HW in abandoned mines, the use of landfills for disposal of HW and other suitable alternative ways are reported. The issue of abandoned mines, with the associated physical, environmental and public safety concerns, constantly emerges around the world as a reminder of the legacy that past mining operations have created. Some abandoned mines give rise mainly to physical concerns. These concerns include public health and safety, visual impacts, stability issues and dust problems. Accidents related to vertical openings or deteriorating structures are the most common cause of death and injury in abandoned mines. Lethal concentrations of explosive and toxic gases like methane, carbon monoxide and hydrogen sulphide can accumulate in underground passages. Rock falls and cave-ins from adits or pit walls can be safety hazards. Unsafe structures include support timbers, ladders, cabins and other related features. Abandoned mines and associated features can also have a detrimental effect on soils, water, plants and animals. The extent of the effects is not fully known because inventories are incomplete and some efforts are still being evaluated. Water is one of the resources most frequently polluted by abandoned mines. Water is also the main conduit by which impacts from abandoned mines extend beyond the immediate site. Elevated concentrations of metals and increased levels of suspended sediment, acidity, hydrocarbons, and brine leaching can threaten surface and underground water quality and aquatic habitats. The socioeconomic consideration of abandoned mines arises mostly from both the physical and the environmental effects discussed in the preceding paragraphs. These include the safety hazards caused by abandoned mines that can result in the loss of lives. Contamination of both ground and surface waters by abandoned mines impacts on the aquatic systems, which affects communities that depend on fishing for their livelihoods. There may also be imposition of restrictions on legitimate users of the waters who may find it unsuitable for irrigation, livestock watering, industrial or domestic use. Funds are required for the rehabilitation of abandoned mine sites. The question when dealing with abandoned mines is: who provides these funds, what mechanisms exist in various jurisdictions to raise these funds, and who is ultimately responsible for the rehabilitation work and the long-term care of the sites. In some cases governments are forced to take on the task of rehabilitation when there are no identifiable owners or if the owners have no resources to pay for rehabilitation. Some mines are situated so that present or past mining operations have caused contamination of the groundwater. For such mines backfilling and sealing for isolation of stored HW can in fact lead to improved environmental conditions. The situation in Europe is defined by the EC Landfill Directive (Council Directive 1999/31/EC of 26 April 1999 on the Landfill of Waste, Commission of the European Communities, Official Journal of the European Communities, 16/7/1999, L 182/1-19), which was adopted in July 1999. It sets out new operational, regulatory and technical requirements for the landfilling of waste. In the past a large amount of HW was co-disposed with non-hazardous waste (NHW)

but this practice had to end. The overall effects of the additional measures within the Directive are to: (i) increase disposal costs, (ii) prohibit the long established practice of co-disposing HW with NHW, and (iii) require the development of additional treatment facilities. Some analysis (Implementation of Council Directive 1999/31/EC on the Landfill of Waste − Second Consultation Paper, Department for Environment, Food and Rural Affairs, London, August, 2001) indicates that hazardous liquid and solid wastes are likely to incur high per ton additional costs. Part of the EC acceptance criteria for HW (Section 2.4 of Commission Decision establishing criteria and procedures for the acceptance of waste at landfills pursuant to Article 16 and Annex II of Council Directive 1999/31/EC on the Landfill of Waste, Commission of the European Communities, Brussels, 01.05.2002) which specifies the leaching limit values for different components of the HW, applies only for landfills for HW and not for underground storage facilities. Therefore, disposal of HW in underground storage facilities would reduce the requirements for treatment of the hazardous solid wastes. There are indications that adaptation of some of the existing abandoned underground mines would be cheaper than building new landfill repositories for disposal of HW, especially taking into account the long-term monitoring of landfills for HW and pollution prevention measures. In many countries disposal of inorganic waste that can contaminate groundwater is presently made in the form of landfills equipped with clay-based top and bottom liners. The longevity of the liners is limited because of erosion of the top liner and chemically induced degradation of the bottom liner, particularly if the pH of the percolate is low. The continuous percolation of the waste mass by rain and meltwater means that the ion-sorbing capacity of the bottom liner is ultimately exhausted so that no further sorption can take place after a certain period of time. The percolate then passes through the bottom liner to the groundwater with the same concentration of contaminating ions as the porewater has in the lower part of the waste mass. By collecting and cleaning the percolate, pollution of the groundwater can be prevented for some period of time; but it is questionable whether the institution responsible will continue to take care of the cleaning operation for decades and centuries and to safely dispose the concentrate that results from the cleaning process. For many of the waste materials that are presently being accumulated on the ground surface, disposal in abandoned mines would offer an alternative option implying very slow or no percolation at all for a very long time perspective. Hence, the only transport mechanism is diffusion; but if solid waste is mixed with even a small amount of expandable clay, diffusive migration of hazardous ions released will be very much delayed. The most important gain achieved by mine disposal is that the long-term impact on the environment will be much smaller than for disposal on the ground surface, and there are also other important benefits such as saving the ground surface for more valuable purposes than waste disposal. Disposal of waste, such as incinerated ash, low-level radioactive waste and contaminated soil, using suitable simple versions of the clay-isolation principle

may not represent higher cost than common landfilling, and the capitalized cost over a long period of time should be lower since no maintenance or monitoring will be required. Ash commonly has, or can be given, a gradation that is suitable for mixing with fine-grained expandable clay-like powder of Friedland Ton. Past experience tells that the dry density can be raised sufficiently to give the mixture a low hydraulic conductivity and a low ion diffusion capacity as well as a certain expandability. Placement of such mixtures in drifts and rooms in abandoned mines using modern backfilling and effective compaction techniques thus means that the clayey ash can not only be effectively isolated from the biosphere but also support can be provided for the rock to avoid convergence of the backfilled rooms and hence settlement of the ground surface, which is a common problem in mined-out areas. It is also proposed that low-level radioactive waste (LLW) with short-lived radionuclides can be disposed in mines, since it requires guaranteed isolation of the waste for a few hundred years. Considering the fact that suitably designed and constructed clay barriers with a thickness of less than 1 m will not even be water-saturated in this period, as shown by our research, the disposal concept described in this book should be acceptable. The high risk of groundwater contamination by geological disposal of waste that can give off radionuclides would still require careful selection of suitable mines and particularly effective isolation potential of the clay barriers. An attractive version of disposal of LLW in mines, for both environmental and cost reasons, would be to apply it in freshly and carefully excavated drifts and rooms in actively used mines while continuing the mining operation in other parts. Where environmental hazards have taken place, of which the Chernobyl nuclear accident is a typical example, large amounts of soil have to be dug out and transported to suitable sites for cleaning or isolation. Other examples are areas where impregnation of arsenic in wood has taken place or where a chemical industry has been located and caused contamination of the soil with heavy metals, pesticides and similar compounds. The quantities of soil that have to be removed can be hundreds of thousands of cubic meters, for which bigger abandoned mines will be suitable. The same principles have to be followed as for disposal of ash and similar preparation of mixtures of waste in particulate form with fine-grained expandable clay powder, preferably using the sandwiching method. Considering the above, a number of suitable mines should be prepared and characterized with respect to the type of contaminated soil that they can store in case of unexpected events. The Editors 2006

CHAPTER 1 Hazardous waste generation and management in Europe D. Kaliampakos1, A. Mavropoulos2 & M. Menegaki1 1

School of Mining & Metallurgical Engineering, National Technical University of Athens, Greece. 2 EPEM, Greece.

Abstract This chapter provides an overview of the hazardous waste generation and management strategies in Europe. The results show that four waste streams require special attention: (i) waste from the waste management industry; (ii) waste from organic chemical processes, more specifically pesticides, due to both their environmental impacts and their importance for the chemical industry; (iii) old batteries; and (iv) the waste from electrical and electronic waste stream. Some issues such as general correlation between GDP and waste from energy production, waste import to EU member states, and the concept of waste hierarchy for waste management are discussed. The relative environmental impact of waste is estimated by using information on the quantity and the degree of hazard associated with it. Waste with a high specific environmental impact per ton is normally found in minor volumes and is therefore more difficult to be separated and collected. Until now, waste management has mainly concentrated on waste streams in the middle of the area marked.

1.1 Introduction The last 10 years have been characterized by major changes in hazardous waste generation and management. Changes in generation rates are not uniform in European countries and they strongly depend on the phase of economic development and the specific industrial sectors that characterize this phase. Some well-developed countries (e.g. Austria) have shown a great increase in hazardous waste generation (62%) while others (e.g. Denmark) have shown a substantial

2 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES decrease (57%). On the other hand, in Ukraine hazardous waste generation has decreased by 38% between 1996 and 2000, while in the Russian Federation quantities have increased by 32% between 1996 and 1999. Such dramatic differences are connected with the legislation and the definition of hazardous waste in each country. The lack of a uniform definition for hazardous waste and consequently the absence of a common classification system result in questionable conclusions regarding the total quantities and the general trends in hazardous waste generation and management. However, in terms of quality there are certain issues that should be taken into consideration. Several studies indicate that a limited number of specific industrial sectors contribute substantially to hazardous waste generation in each country. An EEA study [1] has shown that a large proportion of hazardous waste in most Western European countries consists of a relatively small number of waste types (typically 75% of hazardous waste consists of 20 principal types, a very small number compared to the 236 different hazardous list codes). The major types differ from one country to another, but in most EU countries hazardous waste generation is dominated by a relatively small number of sources. This means that prevention and recycling efforts can be relatively easily focused at specific industries in each country, allowing the possibility of achieving remarkable results within a short period.

1.2 Hazardous waste generation in Europe The EEA member countries generate about 36 million tons of hazardous waste per year [2]. It is extremely difficult to interpret the statistical data on hazardous waste. The analysis of the data shows large changes in reported amounts over time, as illustrated in Table 1.1. Countries and regions with figures for both 1990 and 1995 show an apparent increase (65% on average) in hazardous waste quantities, mainly due to changed definitions and new legislation. Germany, with figures for 1990 and 1993, and UK, with figures for 1990 and 1994, show a decline by an average of 21% before the introduction of the Hazardous Waste List (HWL). This decline can be possibly explained by the introduction of cleaner technologies. The dissociation of waste generation from economic growth is a big challenge, since the detailed analysis of the relationship between those two factors reveals several different trends. For instance, country comparisons show no general correlation between GDP and waste from energy production, which probably reflects national differences in energy supply systems. Coal-fired power plants generate large amounts of fly ash, while hardly any waste is produced from hydroelectric power stations and nuclear power plants generate a small, but extremely hazardous, amount of waste. For hazardous waste a correlation between GDP and waste quantities can be demonstrated according to the data from 1995. Nevertheless, this is not valid for the data from 1990. In this period large changes took place both in awareness of hazardous waste and in definitions and classification procedures. Thus, the apparent correlation in 1995 may be spurious.

HAZARDOUS WASTE GENERATION AND MANAGEMENT IN EUROPE

3

Table 1.1: Reported quantities (in tons) of hazardous waste in selected countries and regions [1–5]. Year Country

1990

Austria Denmark Netherlands Germany (North Rhine – Westphalia)* Germany UK Spain (Catalonia) Spain (Basque Country and Catalonia) Greece

317,000 106,000

1993

1994

1995

1996*

1999*

577,000 252,000 895,000 1,597,671

13,079,000 2,310,000 674,400

9,093,000 2,080,000 831,439 1,362,317

286,856

*Quantities according to the first two digits of HWL codes.

5000

Construction waste R2 = 0.7652

Waste generation (kg per capita)

4500 4000 3500 3000

Manufacturing waste R2 = 0.3857

2500 2000 1500

Municipal waste R2 = 0.6872

1000 500

Hazardous waste R2 = 0.8960

0 –500 0

5000

10000

15000 ECU per capita

20000

25000

30000

Figure 1.1: Correlation between waste generation and GDP per capita [2, 3, 6, 7].

For each member state, waste quantity per capita has been plotted against economic activity related to selected waste streams. Figure 1.1 shows that the generation of municipal, construction and hazardous waste seems to be related with the economic activity behind waste generation whereas such a relation does

4 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 1.2: Total generation of hazardous waste in EEA member countries stated in tons. Generation per capita in kg [2, 4, 6, 8]. Country

Year

Total generation

Generation per capita

Classification

Austria

1992 1994 1995 1990 1995 1993 1992 1995

423,000 513,000 577,000 106,000 250,000 9,100,000 99,000 248,000

54 64 68 21 48 113 28 70

National National National National National National Basel HWL

Denmark Germany Ireland

not seem to exist for manufacturing waste. A good correlation is assumed if R2 values are above 0.7. In relation to municipal waste the economy is stated as final consumption from households in purchasing power standard (PPS). Hazardous waste is related to GDP stated in PPS. Construction and manufacturing waste are related to the part of the GDP originating from construction and manufacturing activities. About 1,665,500 tons of hazardous waste were imported to EU member states and Norway in 1995. The majority of the above waste (approximately 85%) came from other EU member states, 8% came from other OECD countries, in particular Switzerland, US, Norway, Hungary and the Czech Republic, while the sources for an amount of about 6% are unknown. Many non-OECD countries do not have adequate facilities to treat their hazardous waste in a safe way. Until these countries are properly equipped, the EU could help by importing and treating their hazardous waste. However, only 16,000 tons (approximately 1%) of the imports to EU member states and Norway were hazardous waste from non-OECD countries, in particular from South Africa, Brazil, Macedonia and Slovenia. Some more details are provided in Table 1.2. 1.2.1 Hazardous waste generation per employee The industrial structure varies within each country and region. The relative size of manufacturing industries is approximately the same in Denmark and Austria, while its importance in the Basque Country and Germany is greater, when measured by the number of full-time employees. The hazardous waste generated per employee in the manufacturing and other sectors of the countries, for which data were available, is given in Table 1.3. The number of employees in different industrial sectors can explain the difference in quantities of hazardous waste generated only to a limited extent. Nevertheless,


5

Table 1.3: Hazardous waste generated (in kg) per employee in Austria, Denmark, Germany, Ireland and Spain (the Basque Country and Catalonia) according to NACE code [1, 9]. Country Austria (1996) Denmark (1996) Germany (1993) Ireland (1996) – excluding recovery on site Spain/Basque (1994) Spain/Catalonia (1996)

Manufacture

Trade, service, transport and infrastructure

210 144 372 436

223 135 129 628

888 156

49 1348

the generation of waste seems to be more closely related to the number of employees than to the total population. A few dramatic differences in waste per employee may, for certain industries, be explained by the presence of waste types considered hazardous in only one country. 1.2.2 Main waste streams in Europe Almost 80% of the hazardous wastes become from eight activities as outlined in Fig. 1.2. More specifically, waste from the waste management industry and inorganic waste from thermal processes make up more than 36%. Waste from organic chemical processes, inorganic waste from metal treatment and coating of metals, and hazardous waste from construction and demolition have an equal contribution of almost 9% each. Figure 1.3 presents the main waste streams, classified according to their percentage in the top five HWL 6-digit codes. For this purpose, more detailed profiles (based on 6-digit codes of HWL) of several countries have been used. These countries include Austria, Denmark, Ireland, Germany and Spain. According to the data presented in Fig. 1.3 it is clear that: • There is a lack of classified data (according to the HWL) in several countries. Even when there are available data, the use of different classification systems complicates the quantification of the trends in all the countries and regions. This issue has been officially considered as one of the major policy barriers for the development of a European level hazardous waste management. • It is certain that hazardous waste amounts have increased, but it is difficult to quantify the rate of increase, due to lack of relevant data or due to no compatibility. For Austria, Spain/Catalonia and Denmark, the data show increasing quantities of hazardous waste in the period 1993–96 with higher rates of increase for Austria and Spain/Catalonia and smaller rates for Denmark.

6 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Wastes from waste treatment facilities, off-site waste water treatment plants and water industry

20.99%

15.18%

Inorganic wastes from thermal processes

Construction and demolition waste

9.30%

Inorganic waste with metals from metal treatment and the coating of metals

9.18%

8.95%

Wastes from organic chemical processes

5.62%

Oil wastes

Packaging, absorbents, wiping cloths, filter materials and protective clothing

5.59%

Wastes from shaping and surface treatment of metals and plastics

5.29%

0%

5%

10%

15%

20%

25%

Figure 1.2: Main hazardous waste streams in EEA countries.

% on top 5 6-digit codes

35% 28.36%

30% 25% 18.34%

20% 15.66% 15% 10.32% 10% 5% 0%

Wastes from organic Construction and Wastes from thermal Wastes from waste chemical processes demolition wastes processes (code 10) management (code 07) (including excavated facilities, off-site soil from waste water treatment contaminated sites) plants, preparation of (code 17) water for human consumption and water for industrial use (code 19) HWL codes

Figure 1.3: The main waste streams included in the top five HWL 6-digit codes.


7

• However, increasing amounts of hazardous waste can be the result of positive developments such as better collection and registration of waste and not necessarily as a result of a real increase in waste generation.

1.3 Current hazardous waste management in Europe The EU has established the well-known concept of waste hierarchy for waste management. According to this concept, waste prevention and minimization is the only viable long-term solution for waste management, while recycling is the second preferred option. However, these undoubtedly right options must translate into a need to design materials, goods and services in such a way that their manufacture, use, reuse, recycling and end-of-life disposal results in the least possible waste. Thus, this concept requires great changes in economy,market and social behaviours and such changes need time to be prepared and applied. In the mean time, hazardous waste management in Europe is characterized by great differences from country to country. In several Western European countries the main option is recovery of hazardous waste, while in the majority of the EU and European countries landfill or incineration without energy recovery are widely used. In many countries, hazardous waste has to be stabilized before disposal, using an appropriate physicochemical treatment. However, treatment methods are often poorly defined, sometimes they are even undeclared, leading to difficulties in comparing practices and environmental impacts. Tables 1.4 and 1.5, taken from Eurostat [10], provide the latest year available information regarding hazardous waste management activities in Europe. Incineration of hazardous waste is a commonly used practice for disposal in many countries. According to the latest year available data from Eurostat [8], at least 4.72 millions tons of hazardous waste is incinerated without energy recovery, an amount comparable with 5.9 millions tons of hazardous waste that are treated by physicochemical methods. Social acceptance of incineration is a frequent problem, especially in the cases where local conditions eventually prohibit the sustainability of operations of the incineration plants (e.g. long transport routes). Although the specific technique can reduce the after-treatment residue of waste, not all hazardous waste are suitable for safe incineration. Moreover, fluegas cleaning has become a very difficult and very expensive issue, especially for hazardous waste incinerators, after the release of the new EU directive for incinerators. One further important issue is that part of the residue (fly ash and bag-filters) is hazardous waste and needs, in any case, another disposal option. It should be noted that slag and fly ash from waste incineration are two of the major hazardous waste streams in a number of Western European countries. Landfilling of hazardous waste is officially considered the lowest-ranking waste management option. However, it still is the dominant method of disposal in Europe. According to the latest year available data, more than 13.2 million tons of hazardous waste is landfilled, an amount remarkably larger than the sum

8 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 1.4: Recovery operations in hazardous waste management in Europe. Recovery operations

Country

Year

Total

Belgium Denmark Germany Greece Spain France Ireland Italy Luxemburg Netherlands Austria Portugal Finland Sweden UK Iceland Norway Switzerland Bulgaria Czech Republic Estonia Hungary Poland

1999 1998 – 1997 1996 1998 1998 1997 1998 1998 – – 1997 – 1993 1999 1998 1998 1997 1999

634 224

Romania Slovak Republic

1999 1996 1999 1999 1998

Incineration Recycling (energy and recovery) composting

Other recovery operations

156

68

168

1,197 222

208

5 92

629

159

42

19

Preparatory activities

100

153

227

61

92

196 6 119 73 317

78 365 400 414

37

28

3 68

411 158

316

8

of all the other hazardous waste management techniques (11.8 millions tons). Environmental problems, as well as the reluctance among the public to accept landfills as a safe technology, make the establishment of new landfills extremely difficult. In most countries, hazardous waste landfills’ capacities are very limited or unavailable. Thus, pending the availability of treatment and disposal options, hazardous waste is accumulating. Some countries (e.g. Estonia, Latvia) have demonstrated some success in this regard by establishing safe storage for large quantities of obsolete pesticides. However, this cannot be considered as a final solution. The need for an environmentally sound alternative to landfill is more than urgent. Figures 1.4 and 1.5 provide a condensed picture of current practices in hazardous waste management in Europe, as taken by Eurostat.


9

Table 1.5: Disposal–treatment operations in hazardous waste management in Europe. Disposal operations

Country

Year

Belgium Denmark Germany Greece Spain France Ireland Italy Luxemburg Netherlands Austria Portugal Finland Sweden UK Norway Switzerland Bulgaria Czech Republic Estonia Hungary Poland Romania Slovak Republic

1999 1998 – – 1996 1998 1996 1997 1998 1998 1996 – 1997

Total

Physicochemical treatment

Incineration Biological (without energy treatment recovery) Landfill Other 129

631 57

1,132

750 1,361 46 282 – 244 106

189 803 33 791 – 370

3

59

234

185 – 371

931

57

88

686 302 7

557

365

1993 1998 1998 1998 1999 1999 1996 1999 734 1999 1,759 1998

59 620 335 277 1,071

128

7 1,015 416 592

5 0 1,110

103

5 68

219 237 217 5,748 1,035 113 1,318 392

620

10

576 6

436 25

1.4 Trends and expectations 1.4.1 Dangerous substances from waste streams and EU priorities In order to predict future trends, it is more than necessary to take into account not only the distribution of hazardous waste but also the relevant contribution of dangerous substances from current waste management practices as well as EU priorities with regard to waste streams. There are three types of emissions that are of relevance at the global level, namely: • organic micropollutants, particularly dioxins and furans (incineration is still a major generating source);

10 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Recovery

Disposal

Other

Estonia 2000 Estonia 1995 Romania 2000 Romania 1995 Bulgaria 2000 Bulgaria 1995 Ukraine 2000 Ukraine 1995 Czech Republic 2000 Czech Republic 1995 Switzerland 1998 Switzerland 1995 Netherlands 2000 Netherlands 1995 Luxemburg 2000 Luxemburg 1995 Ireland 1998 Ireland 1995 France 2000 France 1995 Denmark 2000 Denmark 1995 Iceland 2000 Iceland 1995 0%

20%

40%

60%

80%

100%

Figure 1.4: Current hazardous waste management in selected European countries. • greenhouse gases, particularly methane (landfilling is one of the most important sources as stated in the EMEP/CORINAIR Atmospheric Emission Inventory Guidebook); • volatile heavy metals (incineration is still a major generating source for specific metals). Emissions of the above substances contribute to a slow but continuous degradation of environmental conditions. Other emissions from incineration, such as polychlorinated biphenyls (PCBs), have a more regional character and are important at the regional/local level.


11

59.52%

60% 50%

43.84%

40% 29.70% 30% 19.60% 20%

15.68% 10.79%

Total treated

Total disposed of

Landfill

Physicochemical treatment

Incineration

Biological treatment

Recovery

0%

5.56%

4.54%

Other

10%

Figure 1.5: Current hazardous waste management practices in Europe.

Landfill emissions other than methane are mainly of local or regional importance. Most of these emissions are emitted in a diffuse manner to the surrounding environment and, in particular, to groundwater. In regions where communities rely on groundwater for public water supply, such emissions, if uncontrolled, can have implications for public health. Organic trace substances produced as a result of biodegradation processes can also be a source of nuisance to local communities as well as a potential risk to human health. For both landfill and incineration, discharge of wastewaters results in relatively high emissions of chloride salts. Table 1.6 [11] provides some interesting remarks regarding the emissions from incineration and landfilling of selected waste streams. In relation to this, it is interesting to note the results of a survey carried out by OECD [12] where 10 European countries were asked about their present and future waste minimization problems and priorities. According to the results obtained (Table 1.7) one of the most important waste streams is waste from electrical and electronic equipment (WEEE). The production of electrical and electronic equipment is one of the fastest growing domains of manufacturing industry in the Western world. New applications of electrical and electronic equipment are increasing significantly. There is hardly any part of life where electrical and electronic equipment are not used. This development leads to an important increase in WEEE. The WEEE stream is a complex mixture of materials and components. In combination with the constant development of new materials and chemicals having environmental effects, this leads to increasing problems at the waste stage.

12 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 1.6: Ranking of dangerous substances from landfill and incineration. Dangerous substances

Source

Category

Remark

Incineration

Landfill

Human toxicity Ecological toxicity Greenhouse Gas Human toxicity Ecological toxicity Eutrophication

HCl Heavy metals As, Cd Salt, e.g. chloride Organic emissions

Incineration Incineration

Acidification Human toxicity

Landfill Incineration Landfill

Ecological toxicity Human toxicity Nuisance

Heavy metals Cd, Ni, Cu, Zn, Pb, Hg

Landfill

Ecological toxicity Human toxicity

Very important, incineration is a major contributor Very important Very important due to transboundary movement Important because of the local contamination of surface and groundwater Important Important, carcinogenicity Important, high loads to surface and groundwater Important for employees and neighbourhood Less important due to the small contribution to total emissions, assumed to be stable in the landfill body

Organic compounds PCDD/PCDF CH4 Volatile heavy metals Hg, Cd, Pb Total N, NH4

Landfill Incineration

The WEEE stream differs from the municipal waste stream for a number of reasons: • The rapid growth of WEEE. In 1998, 6 million tons of WEEE were generated (4% of the municipal waste stream). The volume of WEEE is expected to increase by at least 3–5% per annum. This means that in 5 years 16–28% more WEEE will be generated and in 12 years the amount would have doubled. The growth of WEEE is about three times higher than the growth of the average municipal waste (WEEE Draft Directive). • Because of their hazardous content, electrical and electronic equipment cause major environmental problems during the waste management phase if not properly pretreated. As more than 90% of WEEE is landfilled, incinerated or recovered without any pretreatment, a large proportion of various pollutants found in the municipal waste stream comes from WEEE. • The environmental burden due to the production of electrical and electronic products (‘ecological baggage’) by far exceeds the environmental burden due


13

Table 1.7: Present and future key waste streams in selected European countries. Country

Present key waste streams

Future key waste streams

Austria

Waste oil, lubricants, photochemical No information Sewage sludge Waste oil, end-of-life vehicles Paint sludge, WEEE, sewage sludge No information Waste oil, dredging spoil, CD waste, phosphorogypsum Hazardous waste in general

WEEE, waste medicines, end-of-life vehicles No information WEEE, end-of-life vehicles Waste oil, end-of-life vehicles, PCB, WEEE, medical waste WEEE, end-of-life vehicles, sewage sludge No information Dredging spoil, phosphorogypsum WEEE, scrapped oil installations Packing, beverage containers, metal plating sludge Clinical waste, PCB

Denmark Finland France Germany Italy Netherlands Norway Switzerland UK

Packing, beverage containers, metal plating sludge WEEE, end-of-life vehicles, waste oils

to the production of materials constituting the other substreams of the municipal waste stream. As a consequence, enhanced recycling of WEEE should be a major factor in preserving resources, in particular, energy. In order to address adequately the environmental problems associated with the current methods for the treatment and disposal of WEEE, it is considered appropriate to introduce measures at the Community level that aim, firstly, at the prevention of WEEE, secondly at the reuse, recycling and other forms of recovery of such wastes and, thirdly, at minimizing the risks and impacts to the environment from the treatment and disposal of WEEE. Although the main guideline for WEEE management is separate collection and reuse, recycling or recovery, there is a large part of WEEE, concerning old and not rechargeable batteries, which may need extended disposal, at least for some years, until some new and more effective technologies are well established. Since 1990, mercury consumption in primary batteries has declined significantly in the EU due to the introduction of the Directive 91/157/EEC on batteries and accumulators containing certain dangerous substances. The Directive came into force in 1994. The Directive covers, amongst the other types of batteries, the commonly used alkaline-manganese energy cell, the zinc–carbon battery, the zinc–air button cell as well as the silver oxide button cell and the mercuric oxide battery (two small battery types which also contain mercury). Tables 1.8 and 1.9 present mercury emissions from batteries and other sources.

14 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 1.8: Emission factor for mercury: tons per million population. Source

Western Europe

Eastern Europe

0.0002 0.0044

0.00004 0.0013

0.0019 0.0005

0.0003 0.0003

Batteries Measurement and control equipment Electrical equipment Lighting

Table 1.9: Mercury emissions in Europe (in tons) (1995). Source

Western Europe

Eastern Europe

0.09 1.81

0.015 0.500

0.77 0.21 2.88

0.125 0.121 0.761

Batteries Measuring and control equipment Electrical equipment Lighting Total

1.4.2 Future trends up to 2010 The use of certain chemicals is expected to decline over the next decade in the EU. However, a growth of 30–50% in chemicals output is expected for most of the EU countries by 2010 as a result of increasing economic activity, including road transport and agricultural production (Table 1.10). This anticipated growth could accentuate concerns with respect to human and ecosystem health. Considerable uncertainties exist over both the projections for emissions (and consequently concentrations and depositions levels) and the relationships between exposure and effects; emission uncertainties for dioxin, for example, range from 5 to 20. Nevertheless, it is important to consider the future trends for major groups of persistent chemicals due to the potential risk of significant impacts. Atmospheric emissions, concentrations and depositions have been modelled [13] on a European scale for selected heavy metals, persistent organic pollutants (POPs) and for fine particulate matters (PM10). Emission estimates for 1990 have been prepared within the framework of the joint OSPARCOM–HELCOM–UNECE emission inventory [14] and are used to construct projections for the year 2010. 1.4.3 Emission trends of heavy metals Lead emissions from phasing out leaded petrol (85/210/EEC) have been reduced more than 50%, on average, in the EU and the Accession Countries between


15

Table 1.10: Drivers for chemical use and resulting exposure. Main drivers

Chemical

Source

Food production

Pesticides, Cd, Hg

Transport

Pb Pt, Pd, PAHs organics

Fuel conversion

PAHs, Cu, Cd, Hg, As Cu, Cd, Hg, As

Crop treatment, phosphate fertilizers, seed treatment Petrol additives (in some countries); catalytic converters; incomplete combustion oil refining Incomplete combustion, fly ash Ore processing, zinc refining Waste incineration

Mining, metals industry Consumer goods and products (GDP growth)

Dioxins, furans

1990 and 1996 and further reductions are expected by 2010. The concurrent introduction of catalytic converters, however, will most likely result in increased platinum emissions, either through direct release or in the course of reprocessing. Projections indicate that positive trends from abatement measures, such as improved efficiency and geographical coverage in recycling, are likely to be counteracted by a general increase in economic activity [13]. Thus, the overall cadmium and mercury emissions are expected to increase in EEA countries by 26% and 30%, respectively, between 1990 and 2010. Copper emissions (mainly from mining and smelting activities) have increased by 8% and are unevenly distributed between countries. Policies in the pipeline lead to an appreciable decrease in emissions of lead, copper and mercury in the Accession Countries, although cadmium emissions are expected to increase by about 4% due to an increase in road transport and growth of the chemical industry. Heavy metal and arsenic emissions are expected to be diminished as a result of the reduction of the sulphur content of fuels [following EU legislation COM(97)88] and the switch from solid to liquid fuels [15], which are frequently associated with pyrite, the main sulphur source in coal and lignite. Although the improvements in wastewater treatment techniques and the degree of water treatment connections, as well as the tighter controls on industrial discharges, have led to reduced heavy metal river loads, they have intensified the problem of contaminated sludge disposal. 1.4.4 Emission trends of pesticides and POPs Increases in general economic activity, including agricultural production, are projected to counteract positive trends from abatement measures [13]. Policy measures in the framework of the Integrated Pollution Prevention and Control

16 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES (IPPC) directive and its predecessors are expected to reduce emissions of dioxins/ furans (from large-scale combustion plants) and of PCBs. Measures aimed at reducing energy consumption and/or improving conversion efficiency are also expected to have positive effects. In Western Europe the anticipated growth in road transport is expected to increase polycyclic aromatic hydrocarbons (PAHs, for instance, benzo[a]pyrene) and xylene emissions. In the Accession Countries this will be offset by the introduction of cleaner vehicles, although an expected increase in the annual volumes of incinerated waste will lead to increased emissions of hexachlorobenzene (HCB).

1.5 The effect of Directive 99/31 The European Directive 99/31 raises environmental standards for all types of landfills (municipal, inert and hazardous waste landfills) and pushes hard to wards a big increase of the already high landfill tipping fees. The specific directive imposes stringent operational and technical requirements on landfilling and calls for the reduction in the quantity of the various waste streams entering the landfills as well as for the treatment of all waste prior to landfill. The main scope of this directive is to eliminate landfills. The application of the Landfill Directive is usually accompanied by landfill taxes that increase much more the cost of landfilling. The combination of the new Landfill Directive and the environmental and social problems that characterize landfills has led to a remarkable reduction of landfills from a number of almost 10,000 (1991, 12 countries of Central Europe) to almost 5,000 (1999). Landfill space has become much more limited, landfilling is politically driven to be much more expensive and landfill is considered as the less-preferred option in the EU. Figure 1.6 shows the consequent reduction of landfills in Europe. One very interesting issue is that the Landfill Directive makes a distinction between underground storage and landfill. According the directive, underground storage means a permanent waste storage facility in a deep geological cavity, such as a salt or potassium mine. On the other hand landfill means a waste disposal site for the deposit of the waste on to or into land. Article 3 excludes underground storage facilities from: • The provisions of Article 13, paragraph d. The specific paragraph concerns the need for environmental monitoring and aftercare of landfill sites for about 20 years after closure and stoppage of their operation. • The provisions of Annex 1, point 2, which specifies stringent obligation for leachate management in landfills (collection, treatment, protection of surface water). • The provisions of Annex 1, points 3–5, which specify certain measures for protection of soil and water, such as liners, gas handling and control, etc. • The provisions of Annex 2 that mention specific waste acceptance criteria for landfills.


17

Number of landfills 12000 10000 8000 6000

CEE (12 countries)

4000

WE (14 countries)

2000 EECCA (2 countries)

0 1991

1995

1999

Figure 1.6: Reduction of landfills in Europe [16, 17]. (WE: Austria, Belgium, Finland, France, Ireland, Italy, Luxembourg, Portugal, Spain, Sweden, the Netherlands, Iceland, Norway, Switzerland; CEE: Croatia, Cyprus, Czech Republic, Estonia, Hungary, Latvia, Lithuania, Malta, Poland, Romania, Slovak Republic, Turkey; EECCA: Belarus, Tajikistan) Finally, Article 16 and Annex 2 underline the need for the development of specific waste acceptance criteria for underground storage. The exclusion of underground storage from many of the strict obligations that should be applied for landfills results in a big advantage for underground disposal. While capital and operational cost of landfills have become remarkably higher, in accordance with new, highly technical and environmental standards, the construction and operational standards for underground disposal are much more easy to achieve and the related costs are substantially cheaper compared to landfill costs.

1.6 Waste streams and pollutants of interest 1.6.1 Waste streams of interest A general outline of the hazardous waste profiles in several EU countries has already been shown. Based on these data, as well as on the EU priorities, it is clear that the key waste streams as far as hazardous waste is concerned are the following: • Waste coming from the waste management industry is the main hazardous waste substream. The biggest waste stream is the aqueous liquid waste from gas treatment and other aqueous liquid waste. This waste includes a number of heavy metals and the physical form of this waste makes it appropriate for storage within artificial barriers.

18 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES • Although waste from construction and demolition activities and inorganic waste from thermal processes are of major interest, waste from organic chemical processes should be also considered as a main hazardous waste substream due to their environmental importance. This type of waste has longterm interactions with the environment, its pollutants are bioaccumulative and part of this waste represents the greatest problem of the disposal of outdated pesticides. • WEEE is one of the key future waste streams. This stream also includes a number of heavy metals and there are many difficulties in recovering materials due to lack of appropriate technological advances. Since it is considered a certainity that within the next 5–10 years appropriate technologies will be established, underground mines can provide a perfect medium–term storage option, with very low cost and negligible environmental hazards. The same conclusion can be drawn regarding the old batteries stream, as a part of the rapid increasing (and EU special focus) waste stream of WEEE. In all the above cases, underground mine disposal takes advantage of the very slow groundwater flow at depth and the very long transport paths for heavy metals that might be released. 1.6.2 Pollutants of interest After the decision-making of waste streams of interest, the next step to be taken is the selection of specific pollutants. In order to do this, it is necessary to provide a general outline regarding the dispersion of chemical substances (pollutants) and its effects. 1.6.3 Selection of the pollutants of interest Europe is one of the largest chemical-producing regions in the world, supplying 38% of the global turnover. Since 1993, the chemical intensity of EU GDP has been rising for all chemicals and hazardous chemicals production. There are 20,000–70,000 thousand substances or groups of substances in the European market, many being derived from chlorine-based organic chemistry. Little is known about the toxicities, eco-toxicities or risks from most of these substances. Figures on the quantities of substances produced or marketed are in general of little use for predicting the dispersion and the potential exposures, which are still difficult to estimate due to increasing non-point sources of emissions and recycling processes, despite the improvements in multimedia modelling. The European coverage of monitoring data for halogenated organics in general and for POPs in particular is rather patchy. Information on degradations, transformations, by-products and exposures to mixtures is also poor. Most monitoring programme focus on mobile media (air, water), but often neglect soil, sediments and consumer products. Combustion of fossil and other organic fuels is thought to account for over 90% of the environmental load of the 280 types of carcinogenic PAHs.


19

Emissions of dioxins, such as polychlorinated dibenzo-p-dioxins (PCDD) and polychlorinated dibenzofurans (PCDF), which are mainly from air emissions and waste, are significant, but falling in most countries. As mentioned before, if current trends and policies continue, there could be a growth of 30–50% in chemicals output for most of the EU countries by 2010. Cadmium and mercury emissions are expected to increase by 26% and 30%, respectively, between 1990 and 2010; some countries plan to phase out these substances. Emissions from pesticides and POPs – such as dioxins/furans and PCBs – will continue to decrease, but PAH, HCB and xylene emissions are likely to increase. However, the impact of some emerging trends in the management of chemicals such as eco-efficiency improvements, a shift from products to services, the internalization of external environmental costs into prices via taxes, increased information to the public, increased evidence on low-dose effects, greater use of the precautionary principles, and implementation of the OSPAR/Sintra agreement, the IPPC directive and other international policies could lead to marked reductions in the chemical intensity of European GDP, particularly for those substances of concern. In order to focus on pollutants coming from organic chemical processes, there is a need to have a clearer idea about the chemical substances dispersed in Europe. 1.6.4 Chemical substances Humans and ecosystems are constantly exposed to a mixture of natural and manufactured chemicals, some of which are not necessarily harmful. The ‘chemicals intensity’ [18] and ‘dangerous chemicals intensity’ of the EU economy (production plus imports per unit of GDP) [19] have been increasing since 1993 (Fig. 1.7). Supplying 38% of global turnover, with Western Europe being responsible for 33%, Europe is one of the largest chemical-producing regions in the world and the industry is expected to continue its vigorous growth. In line with the decline in their GDP between 1989 and 1995, the chemical production in the Accession Countries has been decreased; nevertheless it has seen a recovery in more recent years. The higher value-added brands of the sector are expected to flourish, benefiting from increases in both domestic demand and exports. However, the social and environmental costs of harmful environmental and health impacts are difficult to quantify [20] and rarely borne by those responsible for these impacts. Human and ecosystem exposure depend upon the dispersion pattern of chemicals, which is determined by their physicochemical properties, their respective release modes, the environmental medium into which they are first released [21], their reactivity and degradability, and the kinetics of these physical and chemical processes. Certain chemicals, most notably chemical elements, never degrade, while organic substances may have half-lives and environmental residence times ranging from a few days up to geological timescales. Assessment of dispersion and exposure is exceedingly difficult; while processes can be studied in a

20 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES

Index (1990 = 100)

130 120 110 100

1997

1996

1995

1994

1993

1992

1991

1990

90

Estimated EU's production and import of "dangerous chemicals" / "chemicals of concern" (volume). Aggreggated by E.C.B. 1999 EU's total production of chemicals (volume) [CEFIC, 1998] GDP (Gross Domestic Product, EU15) [EUROSTAT]

Figure 1.7: EU production and import of ‘dangerous chemicals’/‘chemicals of concern’ and total chemical production. laboratory, their impact in varied environmental conditions is very uncertain. Data on environmental impacts can only be gathered through extensive and continuing monitoring of both the environmental concentrations of selected substances and their impacts on environmental compartments. A recent workshop on environmental monitoring [22] has emphasized the importance of long time series in order to be able to detect changes with time, but has also highlighted the need to re-evaluate older data with improved scientific insight. Data on the biotoxicity and toxicity of chemicals is very limited (Fig. 1.8). For 75% of large-volume chemicals (marketed in excess of 1000 tons a year) there is insufficient publicly available data even for minimal risk assessment under the OECD guidelines [18]. Figure 1.9 provides a very useful picture in order to clear up the situation regarding our knowledge for these substances. Currently up to 70,000 or more chemical substances are used for different purposes. A significant number of these substances do not occur naturally, but are manufactured, in some cases, in large quantities (HPVCs), with a resulting high statistical probability of human exposure. Many of the HPVCs are used in a vast range of manufactured goods and other products that are considered essential for modern life, including detergents and other ‘down-the-drain’ chemicals. Several hundred new substances are marketed each year and are recorded on the European Lists of Notified Chemical Substances (ELINCS), which has over 2000 substances listed. The European Inventory of Existing Commercial Chemical Substances (EINECS) lists over 100,000 substances which are supposed to have been on the market in 1981. However, only 10,000 are produced in volumes greater than 10 tons/year. There is very little data on the dispersion or fate or effects of most substances.


21

Acute terrestrial toxicity Carcinogenicity Chronic aquatic toxicity

Properties and Toxicities

Fertility Acute algal toxicity Biodegradation Teratogenicity Acute inhalation toxicity In vivo toxicity Acute fish/crustaceous toxicity Physicochemical properties Acute dermal toxicity Chronic toxicity Genotoxicity/mutagenicity Acute oral toxicity 0

10

20

30

40

50

60

70

80

Data availability (%)

Figure 1.8: Availability of data on 2472 high-production volume chemicals (HPVCs) submitted to the European Chemicals Bureau [23].

Aquatic monitoring Long-term toxicity data exist Aquatic priority list Dangerous substances HPV chemicals EINECS 1

10

100

1000

10000

100000 1000000

Figure 1.9: The chemical universe in contrast with some current monitoring and classification activities.

22 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES 1.6.4.1 Chemicals of concern The analysis is focused on chemicals that can be driven to water resources via leakage from hazardous waste storage facilities. The migration behaviour of a chemical along the water path is largely determined by its chemical and physicochemical properties. Redistribution of contaminants between the aqueous and the solid phases is controlled by the prevailing water chemistry and the resulting surface properties. Zones of high acidity or alkalinity (measured by low/high pH) and/or redox potential or high sorption capacity (e.g. clays) can act as geochemical barriers. Indeed, these properties are utilized in engineered landfills to prevent leakage. 1.6.5 Heavy metals Heavy metals are metals or metalloids, which are stable and have a density greater than 4.5 g/cm3, namely lead, copper, nickel, cadmium, platinum, zinc, mercury and arsenic. Human activity generally leads to the dispersion of metals and other elements that have been concentrated by geological processes and over geological timescales. The use of metals, as well as human exposure to metals, has significantly increased since the onset of the industrial revolution and continues to do so on a global scale. Arsenic, cadmium, copper, lead and nickel have been identified as being of the greatest concern. The production and use of heavy metals is driven by a wide variety of industrial, agricultural and domestic uses such as metallurgy, catalysts, pigments for paints, batteries, electronics components, fertilizers, solid fossil fuels, plastics and fuel additives. The major diffuse anthropogenic mercury source, in Germany for instance [24], is the burning of fossil fuels. EU average contributions from agriculture to cadmium emissions are around 1%. Cadmium in phosphate fertilizers is of some concern [25] and is dealt with by national legislation in Finland, Sweden and Austria. 1.6.5.1 Heavy metals in water pathways Direct human exposure to elevated heavy metal concentrations via the water pathway has been of limited importance in many Western European areas, but has regained importance as a result of declining control over the quality of groundwater resources and the distribution system. This may, for example, increase human lead exposure from drinking water, countering the lead solubility control measures for water piping. Exposure to surface water-derived heavy metals might occur indirectly via bioaccumulation in freshwater or estuarine or marine fish consumed by humans. The latter, for instance, accounts for half of the mercury intake in Germany [24]. The increasing abundance of biological wastewater treatment plants throughout Europe leads to a shift of environmental dispersion pathways of heavy metals from effluents to sludges. Sludges are either used as fertilizers (if contaminant concentrations are within legal limits) or are incinerated. River loads have decreased considerably as a result of


23

wastewater treatment [14]. The LOIS studies [26] have confirmed that elevated concentrations of heavy metals in river waters are linked to the presence of highsuspended particle loads and natural or anthropogenic complexants. Heavy metals remobilized from stream sediments are of some concern where drinking water resources are augmented by bank filtration. The ultimate recipients of heavy metals in surface waters are the large marine basins. 1.6.5.2 Heavy metals in soil High heavy metal concentrations in soils tend to be more localized, either from high natural background levels (mineral deposits), or from mining, ore processing and other industrial activities. 1.6.5.3 Heavy metals in food The major pathway for human uptake, after inhalation, is ingestion of plant- and animal-derived foodstuffs. The chemical processes associated with bioaccumulation, both in humans and animals, lead to preferential accumulation in certain tissues. Wahlström et al. [27] concluded that the consumption of fish in Finland can be considered, in general, safe, but their liver and kidneys should be avoided. Human exposure to heavy metals may not only result from dietary uptake but also from smoking. 1.6.6 Persistent organic pollutants The number of chemicals characterized as POPs is unknown, but certainly exceeds those that are listed as important [28, 29] or are included in current monitoring programmes. The term persistent organic pollutants includes ‘chemical substances that persist in the environment, bioaccumulate through the food web and pose a risk of causing adverse effects to human health and the environment’ [29]. 1.6.6.1 Polycyclic aromatic hydrocarbons PAHs comprise a suite of around 280 substances from which 16 have been selected by the EU and the US EPA as priority substances [30, 31]. PAHs are ubiquitous and many have environmental half-lives in excess of weeks or months. They are subject to various chemical and photochemical processes in the environment; some of which result in degradation to less toxic products, while others lead to more hazardous compounds, such as nitrosubstituted PAHs [32]. The major sources of PAHs are fossil and other organic fuels such as wood. Combustion is thought to account for over 90% of the environmental concentrations. Noncombustion processes such as the production and use of creosote and coal tar, though poorly quantified, are potentially very significant primary and secondary sources [30]. Combustion processes have the highest dispersion potential over wide areas, but may significantly decrease as emissions are reduced by IPPC measures, although total emissions are liable to increase with economic activity. Human exposure occurs mainly through inhalation of smoke particles to which the PAHs readily attach. Indeed, certain voluntary practices such as smoking

24 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES and the use of household chemicals such as air fresheners result in significant indoor PAH concentrations and human exposures [33]. 1.6.6.2 Organochlorines dispersal in soil, groundwater and some global-scale problems Chlorine-based organic chemistry has become one of the most important branches of the chemical industry [34] accounting for approximately 55% of the production. The main products are pesticides and biocides as well as components for a wide range of industrial and household goods. A class of chlorinated hydrocarbons released into the natural environment on purpose is those that are intended as plant protection products (insecticides, fungicides, herbicides) and biocides. Active ingredients may be not only chlorinated hydrocarbons but also other organic, metal–organic or metal compounds. Application generally results in a diffuse source of emissions (e.g. from agriculture, or organo-tin anti-fouling paints on ships), but for specific applications linear (e.g. weed control on railways) or point sources (wood protection, sheep dips, accidental spills) may be relevant. Emission factors in industrial applications and household goods vary considerably, but are generally quite low during normal use; there are small losses from the technosphere by means of abrasion, wear or leakages, notably PCBs from electrical installations. PVC-based plastics have been of some concern, mainly due to emissions of additives, such as stabilizers or plasticizers (e.g. phthalates, chlorinated paraffins), in the waste stream and from consumer goods intended for children’s use. The recycling of many PVC-based goods and the better process control in incineration has reduced the impact from dioxin formation in thermal waste treatment. Most lipophilic organochlorines (those that are absorbed by fats) are found in the soil solids (the organic or clay fraction), from where they can migrate into deeper strata. A number of European countries have reported pesticides in groundwater; although there is little reliable information for POPs in general. The pollutants eventually reach the sea via surface waters and, inter alia, by colloid or particle-mediated transport. Acute poisoning of humans by chlorinated hydrocarbons is rare in the European region and usually associated with accidental releases during manufacturing, storage or application. Bioaccumulation [34] and persistence in many environmental media can lead to long-term low-level exposure of non-target species. Health effects on humans and animals from continuous or intermittent long-term exposure to low levels are varied and frequently difficult to attribute. Certain pathological observations, including eggshell thinning in various bird species, skeleton malformation in seals and otters, hormonal (endocrine) or reproductive disturbances in various species, were found to coincide with pesticides in the animal tissue [35]. The continuing use of some active ingredients of concern, for instance DDT in developing countries, results in dispersive input to European regions, even though the respective ingredients have been phased out in Western Europe [29]. Lower acute human toxicity and easier handling for less well-educated farmers


25

might be valid reasons for continuing their use in developing countries [36]. The ever-increasing global trade in plant material (foodstuffs, textiles) provides another, anthropogenic, pathway for transboundary dispersion and possible human exposure in Europe. The overall pesticide use – measured by mass of active ingredient – appears to have been decreasing in most EU countries over the past two decades (Figures 1.10 and 1.11) [37]. Finland 2500 2000 1500

1998

1997

1996

1995

1994

1989

1984

1000

Sweden

1998

1997

1996

1995

1994

1989

1984

4500 3500 2500 1500 500

Germany 40000 35000 30000

1998

1997

1996

1995

1989

1984

25000

France

105000 95000 85000

1998

1997

1996

1995

1994

1989

1984

75000

Spain

1998

1997

1996

1995

1994

1989

1984

115000 105000 95000 85000 75000

Figure 1.10: Pesticide consumption in selected countries of EU (in tons of active ingredients).

26 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES As shown in Fig. 1.11, pesticide consumption in the various EU countries does not follow a uniform trend, being a function of agricultural activity and legislation of certain substances. Absolute levels reflect the size of the countries well as the respective importance of the agricultural sector. Consumption in terms of mass, however, does not necessarily reflect environmental impact, as more active and more specific substances are being developed. As far as the DDTs and lindanes are concerned, their production and use have already been reduced or prohibited a long time ago. Nevertheless, it will take considerable time for the reservoirs in various environmental compartments to become depleted and for stockpiles to be exhausted.

Herbicides

Fungicides

Insecticides

Other pesticides

Uk (f) Sweden (f) Spain (f) Portugal (d) Netherlands (a) Luxemburg (c) Italy (b) Ireland (d) Greece (a) Germany (f) France (e) Finland (f) Denmark (e) Belgium (a) Austria (d) 0%

20%

40%

60%

80%

100%

(a) 1980 (b) 1990 (c) 1991 (d) 1992 (e) 1993 (f) 1994

Figure 1.11: Percentage consumption of pesticides according to their types.


27

1.7 Conclusions From the analysis presented above it is concluded that four waste streams require special attention: • Waste coming from the waste management industry. • Waste from organic chemical processes. More specifically pesticides should be considered as a waste stream of major importance, due to both their environmental impact and their importance in the chemical industry. • Old batteries. • The rapid increasing (and EU special focus) waste stream of WEEE.

Volume of flow in tons

The relative environmental impact of waste is related to both the quantity and the degree of hazard associated with it. There are, therefore, two aspects as far as waste generation is concerned: (i) quantitative, i.e. how much is generated, and (ii) qualitative, i.e. the degree of hazard. This is presented for a selection of materials in Fig. 1.12. Waste with a high specific environmental impact per ton is normally found in minor volumes and is therefore more difficult to be separated and collected. Until now, waste management has mainly concentrated on waste streams in the middle of the area marked. Figure 1.13 ensures that heavy metals and pesticides are of major importance, due to their enormous environmental impact. Finally, regarding the selection of pollutants of high importance, two pollutant categories have been selected. First, heavy metals coming from the waste management industry waste, such as incineration slag or from old batteries. The contribution of batteries to heavy metal emissions has already been mentioned before. Some more details are given hereinafter for waste coming from the waste management industry.

water total material throughput sand and gravel

carbon timber

fossil fuels

steel aluminium fertiliser

paper nutrients PVC

solvents heavy metals

hazardous chemicals pesticides

Specific environmental impact (per ton of material)

Figure 1.12: Environmental impacts per ton of waste materials [38].

28 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES 100

-40 -60

HCH

PCP

HCB

PCDD/F

-20

Atrazin

0

Endosulfan

XYL

PCB

Pb

20

Cu

40

Hg

60

Cd

Projected percentage change 1990 to 2010

Accession countries

PAH

EU

80

-80

Substance

Figure 1.13: Projected percentage changes (1990–2010) in emissions of selected chemicals. Table 1.11: Comparison between slag and soil parameters. Concentrations (mg/l)

As Hg Cd Cr Cu Ni Pb Zn PAH

Range in slag

Range in natural soils

0.12–189 0.02–7.75 0.3–70.5 23–3.170 190–8.240 5–500 98–13.700 613–7.770 13–19.000

1–50 0.01–0.3 0.01–0.70 1–1000 2–100 7–4.280 2–200 10–300

Dutch value for good soil quality 29 0.3 0.8 100 36 35 85 140 1

Based on available information, the total amount of slag from incinerator plants is estimated to be between 6 and 9 million tons per year in EEA countries. In a number of countries the slag is recycled and used for road construction, embankments and noise barriers as well as for concrete production. In Denmark and the Netherlands the percentage of slag that is recycled is between 85% and 90%, while only 50% is recycled in Germany and hardly any slag is recycled in Sweden [39, 40]. When analysing the chemical composition of incinerator slag a major concern is the heavy-metal content which in many cases is consider ably higher than the concentrations occurring naturally in soil (Table 1.11).


29

This means that in many cases the use of slag for construction purposes may in the long-term lead to contamination of surrounding areas with dust containing heavy metals, if the surface is not sealed. On the other hand, its use under asphalt or concrete could reduce this problem. In relation to the contamination of water, most of the heavy metals are present as very stable and insoluble chemical compounds. Studies of leaching from slag show that the main risk of contamination of drinking water comes from lead and cadmium, but high contents of soluble chloride and sulphate also constitute a problem. Copper is particularly toxic for marine organisms [41]. Due to its potential for environmental pollution, recycling of slag calls for regulation and strict control of the amounts used, the conditions for use and possibly pretreatment so as to reduce the amount of contaminants in the slag. The identified problems highlight the need for continuous reduction in the use of heavy metals and improved sorting of the waste before incineration. Second, organochlorines are suggested as the pollutants selected from the outdated pesticides waste stream.

References [1] European Environment Agency (EEA), Hazardous Waste Generation in Selected European Countries – Comparability of Classification Systems and Quantities, Topic report No. 14/1999. [2] OECD, Environmental Data Compendium, Paris, 1997. [3] NRCs, Responses from National Reference Centers to questionnaires from European Topic Center on Waste, 1998. [4] Junta de Residus (EPA-Catalonia), Information to the European Topic Center on Waste. [5] National Technical University of Athens (NTUA), Hazardous Waste Inventory in Greece, Athens, 1999. [6] OECD, National Accounts, Vol. II, 1997. [7] NRCs, Comments to the European Environment Agency from National Reference Centers on Waste to draft figures for the waste chapter, July– October 1998. [8] EUROSTAT, New Cronos Database, January 1999. [9] ETC/W, Baseline Projections of Selected Waste Streams, European Topic Centre on Waste, Methodology Report, 1998. [10] EUROSTAT, New Cronos Database, 2002. [11] European Environment Agency (EEA), Hazardous Waste Generation in EEA Member Countries – Comparability of Classification Systems and Quantities, Topic report No. 14/2001. [12] European Environment Agency (EEA), Dangerous Substances in Waste, Technical report No. 38, EEA, Copenhagen, 2000. [13] European Commission, Economic Assessment of Priorities for a European Environmental Policy Plan, Report prepared by RIVM, EFTEC, NTUA


[14] [15] [16] [17] [18] [19] [20]

[21] [22] [23] [24]

[25] [26] [27] [28] [29] [30]

and IIASA for Directorate General XI (Environment, Nuclear Safety and Civil Protection), 1999. UBA, Daten zur Umwelt – Der Zustand der Umwelt in Deutschland, Umwelt-bundesamt, Erich Schmidt Verlag: Berlin, 1997. UNECE, Draft Protocol to the Convention of Long-Range Transboundary Air Pollution on Persistent Organic Pollutants, UNECE Rep. EB.AIR/ 1998/2, p. 52, 1998. Austrian Federal Waste Management Plans. Federal Waste Management Plan, Federal Waste Management Report, Federal Ministry of Agriculture and Forestry, Environment and Water Management, Vienna, 2001. European Environment Agency (EEA), Europe’s Environment: The Second Assessment, Copenhagen, 1998. EEA/UNEP, Chemicals in the European Environment: Low Doses, High Stakes? EEA and UNEP Annual Message 2 on the State of the Environment, Copenhagen, Geneva, 1998. Lindholt, S., Unpublished report for the European Environment Agency based on CEFIC, 1998. Holland, A., O‘Connor, M. and O’Neill, J., Costing Environmental Damage: A Critical Survey of Current Theory and Practice and Recommendations for Policy Implementations, European Parliament/STOA, Report PE 165 946/2, Luxembourg, EP/STOA, 1996. Mackay, D. et al., The multimedia fate model: a vital tool for predicting the fate of chemicals. Environ. Toxicol. Chem., 15, pp. 1618–1626, 1996. OECD, Workshop on Improving the Use of Monitoring Data in the Exposure Assessment of Industrial Chemicals, Berlin, Germany, 13–15 May 1998. Van Leeuwen, J.C. et al., Risk assessment and management of new and existing chemicals. Environ. Toxicol. Pharm., 2, pp. 243–249,1996. Länderausschuß für Immissionsschutz (LAI), Immissionswerte für Quecksilber/Queck-silberverbindungen – Bericht des Unter-suchungsausschusses‚ Wirkungsfragen, LAI-Schriftenreihe, Vol. 10, Erich Schmidt Verlag: Berlin, 1995. OECD, Fertilizers as sources of cadmium. Proc. Cadmium Workshop, 16–20 October 1995, Saltsjöbaden/Sweden, Paris, 1996. Land-Ocean Interaction Study (LOIS), LOIS Content, http://www.pml.ac.uk/ lois/index.html Wahlström, E., Hallanaro, E.-L. & Manninen, S., The Future of the Finnish Environment, Finnish Environment Institute: Helsinki, Edita, 1996. UNEP. Persistent Organic Pollutants: A Global Issue, http://irptc.unep.ch/ pops/ UNECE. Draft Protocol to the Convention of Long-Range Transboundary Air Pollution on Heavy Metals, UNECE Rep. EB.AIR/1998/1, 1998. Howsam, M. & Jones, K.C., Sources of PAHs in the Environment (Chapter 4). The Handbook of Environmental Chemistry, Vol. 3: Anthropogenic Compounds, Part I: PAHs and Related Compounds, Chemistry, eds. A.H. Neilson & O. Hutzinger, Springer: Berlin, pp. 137–174, 1998.


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[31] Keith, L.H. & Telliard, W.A., Priority pollutants: I – A perspective view. Environ. Sci. Technol., 13, pp. 416–423, 1979. [32] Harvey, R. & Jones, K.C., Environmental chemistry of PAHs (Chapter 1). The Handbook of Environmental Chemistry, Vol. 3: Anthropogenic Compounds, Part I: PAHs and Related Compounds, Chemistry, eds. A.H. Neilson & O. Hutzinger, Springer: Berlin, pp. 1–54, 1998. [33] Nolte, R.F. & Jonas, R., Handbuch Chlorchemie I: Gesamtstoffluß und Bilanz, UBA Texte 55/91, Umweltbundesamt: Berlin, 1992. [34] Blomkvist, G. et al., Concentrations of SDDT and PCB in seals from Swedish and Scottish waters. AMBIO, 21(8), pp. 539–545, 1992. [35] Swedish Environmental Protection Agency. Pollutants, http://www.internat. naturvardsverket.se/ [36] Koss, V., Umweltchemie, Springer: Berlin, 1997. [37] Thyssen, N., Pesticides in groundwater: an European overview. Forum Book, ed. IHOBE, 5th International HCH and Pesticides Forum, 25–27 June, 1998, Bilbao, pp. 45–54, 1999. [38] Steurer, A., Material Flow Accounting and Analysis, Statistics Sweden: Stockholm, Sweden, 1996. [39] Danish Environmental Protection Agency (DEPA), Waste Statistics 1996, Environmental Review no. 4, 1998. [40] International Ash Working Group, Municipal Solid Waste Incinerator Residues, 1997. [41] Thygesen, N. et al., Risikoscreening ved nyttiggørelse og deponering af slagger, Miljøprojekt no. 203, Danish EPA: Copenhagen, 1992.



CHAPTER 2 Need and potential for underground disposal – survey of underground mines in Europe D. Kaliampakos1, A. Mavropoulos2 & M. Menegaki1 1

School of Mining & Metallurgical Engineering, National Technical University of Athens, Greece. 2 EPEM, Greece.

Abstract This chapter considers the need as well as potential for disposal of hazardous waste in underground mines and provides a comparison between surface and underground hazardous waste disposal including typical costs. A survey on underground mines in Europe is provided including some that are currently used or considered for disposal of hazardous waste in the future. The survey shows that the number of deep mines that are suitable for disposal of hazardous waste is large in Europe, especially considering that a certain number of currently used mines are expected to cease their operation in the near future. In particular, 15 EU countries are included in this survey: Austria, Belgium, Denmark, Finland, France, Germany, Greece, Ireland, Italy, Luxembourg, Portugal, Spain, Sweden, Netherlands and UK. This does not mean that the number of suitable mines in other European countries is negligible, but it only indicates that at this moment there is no sufficient data to report. It is expected that the number of suitable underground mines for hazardous waste disposal in Eastern European countries would be quite high, which offers an alternative and affordable way of dealing with hazardous waste in these countries.

2.1 Surface vs. underground hazardous waste disposal facilities Underground hazardous waste disposal facilities present some significant advantages compared to the respective surface installations, which can be summarized

34 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES as follows [1]: • Underground facilities take advantage of the protection, isolation and security of the site. Proper design and geological siting can provide very low probabilities of hazardous substances leakage and of any such leakage to the surface environment. • Underground structures are naturally protected from severe weather (hurricanes, tornadoes, thunderstorms, and other natural phenomena). Underground structures can also resist structural damage due to floodwaters, although special isolation provisions are necessary to prevent flooding of the structure itself. Moreover, underground structures have several intrinsic advantages in resisting earthquake motions and they tend to be less affected by surface seismic waves than surface structures [2]. • An underground hazardous waste disposal facility eliminates substantially the visual impacts, which can be of major concern in a surface structure adjacent to residential areas. • Environmental monitoring is limited mainly to air quality within the working area. Other needs for monitoring (e.g. groundwater quality) can be determined during risk assessment. • Long-term and after-care monitoring are usually not necessary since the main protection is provided by the geologic medium. On the contrary, in a surface hazardous waste disposal facility the protection measures have limited lifetime. Thus the landfill should be always monitored for possible leaks, even after the end of operation. • During the operation of a surface hazardous waste disposal facility, the main cost drivers are monitoring, wastewater treatment and financial insurance. According to the above-mentioned characteristics of the underground space, operational cost is expected to be cheaper in the case of underground hazardous waste disposal. • Moreover, in the case of an existing underground space, as it is an abandoned underground mine, there are some additional benefits that strengthen hazardous waste underground disposal, with the most important being the land cost and construction savings. A more detailed comparison between surface and underground hazardous waste disposal facilities is given in Tables 2.1 and 2.2, while in Table 2.3 an indicative sealing cost for a surface installation, as well as the respective cost for an underground hazardous waste disposal facility are presented. It should be noted that with the use of the techniques selected for the LowRiskDT Project, the difference between surface and underground disposal of hazardous waste would increase.

2.2 Survey of underground mines in Europe The economic growth that has been observed in all developed European countries since the industrial revolution relied largely on mining activity. This activity

Table 2.1: General and construction issues in surface vs. underground hazardous waste disposal facilities. Surface HW disposal facility General issues Availability of space Sitting

Construction issues 5 m artificial geological barrier or equivalent barrier (99/31 EC) below the waste body Leachate collection system (LCS) Wastewater treatment

Storm water management

Very difficult due to technical and social issues. Difficult

Hundreds of abandoned underground mines may be suitable. Easier Depends on country.

Necessary

Not necessary, the use of artificial barriers is limited and it depends on risk assessment.

Necessary, because rainfall creates huge quantities of polluted leachate. Normally LCS constitutes of extended piping and drainage layer. Necessary. Treatment level depends on local conditions and potential impacts at water tables and most of the times should be a third level one. Necessary, one of the basic components of design and construction.

Not necessary if water does not enter the waste body. A kind of LCS should be constructed for potential leaks. Most of the time, negligible or no wastewater is generated. Safe storage of wastewater and transfer to wastewater treatment facilities is an indicated solution. Depends on the underground mine conditions – may also be negligible.

NEED AND POTENTIAL FOR UNDERGROUND DISPOSAL

Licensing

Limited

Underground HW disposal facility

35

Surface HW disposal facility Operational issues Stability Environmental impacts of possible major accidents (SEVESO) Environmental monitoring

In situ treatment options Long-term–after-care monitoring

Cost issues Construction cost

Operational cost

Underground HW disposal facility

Crucial point for the waste body formulation. High impacts to water and ground/soil. Toxic gases emissions are considered as a high level hazard. Extended monitoring is necessary, especially for water and air quality. The sensitivity of the surrounding ecosystem and natural resources determines more specific areas that should be monitored. Easier All the protection measures have limited life-time, thus the landfill should be always monitored for possible leaks, even after the end of operation.

Crucial point for the underground space. Limited or no impacts to water and ground/soil system. Toxic gases emissions may create problems to workers. Monitoring is limited to air quality, within the working area. Risk assessment determines other needs for monitoring.

Artificial barriers, wastewater treatment, leachate collection system, gas collection and treatment system, storm water management and excavations are the main components. Monitoring, wastewater treatment and financial insurance, are the main cost drivers.

The components may be the same, but they will probably be cheaper due to limited water entry and utilization of already available space.

More difficult due to space limitations. The main protection is provided by the use of underground space – the deeper the better. After-care monitoring is not necessary.

It is expected to be cheaper.


Table 2.2: Operational and cost issues in surface vs. underground hazardous waste disposal facilities.


37

Table 2.3: Typical sealing cost in surface and underground hazardous waste disposal facilities.

Quantity

Unit

Cost per unit (euros)

8.5

m3

10

85

1

m2

0.002

1

m

2

2 6

2 6

– 0.5

1 0.5

m2 m3

2 5

2 2.5 97.5

1 1

m2 m2

15 32

Thickness (m)

Cost per m2 (euros)

Bottom layer for surface installations Clay barrier (hydraulic conductivity < 10–9 m/s) Geotextile HDPE geomembrane (hydraulic conductivity < 10–9 m/s) Geotextile Drainage layer Total cost

5

–

Sealing for underground facilities HDPE geomembrane 0.002 Shotcrete 0.1 Total cost

15 32 47

was reflected in a large number of mining exploitations, many of which were underground mines. However, the decline of the mining industry during the last decades has led to the closure of many mining sites throughout most European countries. As a result, there are many abandoned underground mines which most of the times remain inactive and practically useless. In addition, due to the continuous decline of the mining industry, a large proportion of the remaining underground mines are expected to cease their operation in the near future [3, 4]. These mines could also be considered as potential disposal sites. A profile of the mining activity has been formulated for all the 15 EU countries [5]. The profile consists of some general data concerning mining activities, active mines and mineral production, active and inactive mines etc. Special emphasis has been given to identify the underground mines in order to look for more details. More than 70 underground mines were registered and their main characteristics were recorded. Most mines are located in Germany, Sweden, Finland, and the UK, as expected due to the intense mining activity in these countries (Fig. 2.1). In addition, an inventory of inactive underground mines, presently used as waste disposal sites, has been carried out. Both of the previous results are presented hereinafter.


Figure 2.1: Distribution of abandoned underground mines.

2.3 The profile of mining activity in 15 EU countries 2.3.1 Austria Although the mining industry has maintained a long tradition in Austria, the metal mining sector is declining, principally due to high operating costs, low ore grades, environmental problems and increased foreign competition. This is not the case with the industrial minerals sector, which produces a number of important minerals. Austria is considered to be a significant world producer of graphite, magnesite and talc [6]. Because of Austria’s long history of minerals exploration and mining tradition, geologic conditions are fairly well known. Future mining activities will most likely be concentrated in industrial minerals, mainly for domestic consumption. The chances of finding new and workable base metal deposits are probably remote.


39

No specific information could be retrieved on inactive mines of the country except Schmitzbe coal mine, which closed in 1995, and Trimmelkam, which closed in 1992. 2.3.2 Belgium Although Belgium has a significant mineral-processing industry, it does not produce minerals as a result of mining activities. In fact, Belgium has no economically exploitable reserves of metal ores or primary energy. Belgium has a significant industrial minerals sector and is an important producer of four groups of industrial materials: carbonates, including limestone, dolomite, and whiting; synthetic materials in the form of soda ash and sodium sulphate; silica sand; and construction materials, including a wide range of different types of marble [6]. Following the closure of the last coal mines in 1992, the only mining operations left in Belgium in 1998 were for the production of sand and gravel and the quarrying of stone, principally specialty marbles and the Belgian blue-grey limestone called ‘petit granit’. Very little information has been retrieved about inactive mines in Belgium. The only abandoned mines found are some coal mines located throughout the country. 2.3.3 Denmark Denmark’s mineral resources are, mainly, the natural gas and petroleum fields in the North Sea that, together with renewable energy, have made Denmark a net exporter of energy since 1996. Most of the mineral commodities produced in Denmark are exported with the majority shipped to EU countries. The mining and metal industry works closely with the Ministry of Environment and Energy, the Danish Environmental Protection Agency, local and community governments, and citizen groups to minimize any adverse effects to the environment. Environmental protection is the main focus of the Danish Environmental Protection Agency. A common goal of the steelworks and other industrial concerns is to make use of as much raw material taken into the plant as possible and to maximize the use of any by-products, such as flue dusts. Denmark has large reserves of non-metallic materials such as chalk, diatomaceous earth, limestone, and sand and gravel. Approximately one-third of the bedrock area in Denmark consists of chalk and limestone. Denmark’s industrial minerals sector is based mainly on these easily accessible materials. Cement, chalk for paper filler, ground limestone and lime, including agricultural and burnt, are produced [7]. As far as sand, gravel and aggregates are concerned, from the mid-1980s to the mid-1990s, the industry was suffering from low prices and fierce competition. However, due to the upswing in the Danish building and construction industry, the industry is now in a healthier shape.

40 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Denmark is the only commercial producer of moler, which consists of a natural mixture of diatomite and 20–25% bentonite. Moler has a variety of applications, such as industrial absorbers, brake linings, and fertilizers, and is an important ingredient of insulation bricks [6]. No specific information could be retrieved on the inactive mines of the country. 2.3.4 Finland Mining history in Finland dates back to 1540, when the quarrying of iron ore commenced in the southern part of the country. Since then, about 260 metallic mines have been operated, with the total amount of ore extracted being around 250 Mt. Finnish metallurgical technology and manufacturers of mining equipment are well-known throughout the international mining community. The exploitation of copper, nickel, cobalt, zinc and lead ores as well as chromium, vanadium and iron deposits has provided the raw material base for the country’s metal industry, with significant processing and refining of copper and nickel concentrates at Harjavalta, zinc at Kokkola, chromium at Kemi by the Outokumpu Group and iron at Raahe by Rautaruukki Oy. The major industrial minerals mined in Finland are apatite, talc and, to a lesser extent, limestone [8]. On 1 January 1995, Finland acceded to the EU. At that time, amendments to the Finnish Mining Law concerning reciprocity took effect and allowed any individual corporation or foundation having its principal place of business or central administration within the EU, to enjoy the same rights to explore for and exploit mineral deposits as any Finnish citizen or corporation. This encouraged foreign investment and increased exploration activities of major and junior companies. Exploration emphasis was given on base metals, diamond, and gold deposits. There are many inactive mines in Finland. Data are included in the websites of Geological Survey of Finland and Outokumpu Oy, which is the leading company in the country. However, due to the lack of available data it could not be specified whether they are open-pit or underground mines. 2.3.5 France France is a major European mineral producer. The traditional mineral industries have been in a state of transition a few years ago. In the past, the heavy economic and political involvement of the state was one of the main elements of the national mineral policy. During the last years, efforts have been made to promote the private sector and to reduce the dependence of state-owned companies on subsidies. The government proceeded with a programme of privatization involving large state-controlled companies to reduce the direct role of the Government in the economy. Among the nine major companies privatized since 1994, the Péchiney Group, Rhône-Poulenc S.A., Société Nationale Elf Aquitaine, and the Usinor Group were included [6].


41

Several industries, such as bauxite, coal, iron ore, and uranium, have steadily undergone changes during the past few years, especially bauxite, which is no longer mined. The iron ore basin of northern France stretches from Lorraine northward into Belgium. For many years, the high phosphorus and low iron content of the ore limited its desirability and the production has been declining for several years. Terres Rouges Mine, the last iron ore mine in the Lorraine district, closed in 1998. French bauxite production ceased altogether by the end of 1993. Mining of lead and zinc completely ceased in France. The two working potash mines, Amelie and Staffelfelden, will be closed until the end of 2004 [9]. All underground coal mines were closed in the Midi-Pyrénées region and in the Nord Pas-de-Calais Basin. Mining in La Mure (Isére) and Carmaux (Tarn) ceased in 1997 [6]. Charbonnages de France envisioned the final stoppage of all coal mining in France by 2005. 2.3.6 Germany The minerals and metals industry, which includes industrial processing, construction, and the mining industry, contributes almost 1% to the GDP. Production in the mining and metals industries depends on a variety of forces, including the availability of materials, as well as the supply and demand. The easing of the worldwide recession is a positive factor for those industries that depend on the exportation of their products. The high costs of production in Germany compared with those of competing foreign producers and the problems caused by trying to balance production between the merged German Democratic Republic and Federal Republic of Germany led to constraint production [6]. The technological standard of German mining operations is world class. Notwithstanding the general contraction of the industry, the production levels of certain minerals remain important, both domestically and on a global scale. For example, lignite ranks 1st in the EU and in the world; marketable rock salt and potash, 1st in the EU and 3rd in the world; and hard coal, 1st in the EU and 11th in the world. There are a large number of inactive mines located in Germany. It should be specified though that there is not much information about their present condition. 2.3.7 Greece The mining and metal-processing sectors of the economy of Greece are small but important parts of the national economy. The mining sector’s share of the gross national product is 1.7%. They are highly concentrated, as five mining companies handle approximately 60% of the sector’s turnover. Bauxite is the most important of the Greek mineral commodities. Other important commodities are chromite, gold, iron, lead, nickel, and zinc [6]. Greece is the largest producer of bauxite and nickel in the EU. Northern Greece is thought to contain a significant amount of exploitable mineral resources and is receiving more attention with regard to exploration activities.

42 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES In 1998, most activities were directed toward gold. A number of multinational companies, such as Rio Tinto Plc., Normandy Mining Ltd., and Newmont Inc., expressed their interests in Greece’s northern territories [10]. The Kassandra Mines (Skouries and Olympias deposits) in northern Greece have been producing lead, silver, and zinc for more than 30 years. The mines were bought in 1996 by TVX Hellas, an affiliate of TVX Gold Inc. of Canada, with the idea of exploiting the refractory gold ore by incorporating pressure oxidation technology into the ore-processing phase. To date, the extracted ore could not be processed, due to the opposition of the residents from nearby areas, who were against the operation of a processing plant due to environmental problems. General Mining & Metallurgical Co. S.A. a ferronickel producer, was the latest state-owned company to be put up for sale by the Greek Government. LARCO was one of the world’s highest cost producers of nickel in ferronickel. Greece is the world’s second-largest producer of bentonite after the USA. Bentonite is extracted from the island of Milos by open-pit mining. S&B and Mykobar Mining Co. S.A. (acquired by S&B in March 1999) are the major producers and accounted for almost all of the Greek bentonite. S&B, together with its affiliates, is the largest producer of perlite in the EU. Perlite is extracted from the island of Milos by Otavi Minen Hellas S.A. (purchased by S&B in 1998). S&B continued also the production of natural zeolite in northern Greece. Lava Mining and Quarrying Co. S.A. (LARCO), specializes in industrial minerals with production of gypsum from the island of Crete, pozzolan from Milos, and pumice from the island of Yali. Grecian Magnesite S.A. is a leading magnesite producer in the western world and the biggest exporter in the EU. Its open-pit mine is at Yerakini in northern Greece. The Greek marble industry plays a leading role in the international dimension stone market, as a result of the marble production in almost all areas of the country, its variety of uses and many colours (ash, black, brown, green, pink, red, and multicoloured). PPC is the major producer of lignite, the predominant fuel in electricity generation in Greece. PPC continued exploration in the basins of Amyntaion, Elasson, Florina, Megalopolis, and Ptolemais. PPC had reserves estimated to be 6.8 billion tons from which 4 billion tons was estimated to be economically recoverable by open-pit mining. Most PPC lignite is produced from the Ptolemais-Amyntaion basin with lesser amounts from the Megalopolis basin. There are various inactive mines in Greece among which there are four underground mines. 2.3.8 Ireland The exploitation of minerals in Ireland has a long history with small-scale production up to 1969. In that year the large complex lead–silver–zinc–copper– barite Tynagh deposit was discovered and several others followed [11].


43

Ireland is a major EU producer of zinc and an important producer of alumina, lead, and peat. Although the range of minerals exploited in the country has been limited, exploration activity for new mineral resources is continually increasing, mainly emphasized in gold, lead, and zinc. The country’s mineral-processing industry is small, as is the demand and consumption of mineral products [6]. Today, there are only three active mines in Ireland: the Tara mine, the Galmoy and Lisheen mine. Industrial mineral production in Ireland is rather low with gypsum and limestone (production of about 1 million tons) being the most important. There are four inactive mines in Ireland, three of which are underground. There are also two inactive mines, but no information was found on whether they are underground or open-pit. 2.3.9 Italy Italy is a significant processor of imported raw materials, as well as a significant consumer and exporter of mineral and metal semi-manufactured and finished products. It is the world’s largest producer of pumice and related materials, producing almost one-half of the world’s output, as well as the world’s largest feldspar producer, producing about one-fourth of the world’s output. The country is the world’s eighth and tenth largest producer of crude steel and cement, respectively. Italy is also an important producer of dimension stone and marble [6]. Growth in Italy’s mining and extractive industries was marginal in 1998. Among the metallic ores, lead was mined, although production was minimal and decreasing. Most of the output came from the Silius Mine in Sardinia. The small output of zinc ore came from the safety and environmental recovery work in the remaining sites in the Iglesias area of Sardinia. Industrial mineral production is the most important sector. Italy is the second largest cement producer of the EU, after Germany. Italcementi-Fabbriche Riunite Cemento S.p.A. is the largest cement producer in Italy with 28 plants and more than 30% of the Italian market. Italy is famous for its marble, which occurs in many localities and is quarried by hundreds of different companies. In 1998, production of potash remained suspended. The main reasons were the result of a severe drought that has restricted the availability of process water to the plants and the inability to remove waste material and mine water owing to environmental and ecological concerns. In Sicily, the underground mines that were operating at Pasquasia, Racalmuto, and Realmonte, remained on standby. Mining of metallic ores is expected to remain at its reduced level because of ore depletion. The metals-processing industry, based primarily on imported stocks, is expected to continue to play an important role in Italy’s economy. Italy is expected to remain a large producer of crude steel and a significant producer of secondary aluminium in the EU. The industrial minerals quarrying industry and preparation plants are expected to remain significant, especially in the production of barite, cement, clays,

44 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES fluorspar, marble, and talc. Italy is expected to continue to be the world’s leading producer of feldspar, feldspathic minerals, and pumice. The ceramics sector is expected to be important, particularly regarding exports. 2.3.10 Luxembourg Luxembourg’s mineral industry consists principally of raw materials processing information systems, and trading, among others. The country produces traditionally sand and gravel and crushed and dimension stone. Mining in Luxembourg is represented by small industrial mineral operations that produce material for domestic consumption. These minerals include dolomite, limestone, sand and gravel, and slate [6]. ARBED dominates the mineral industry and is involved in producing pig iron, crude steel, and stainless steel, all from imported material. The company specializes in the production of large architectural steel beams and is involved in other areas of the economy, such as the cement and brick-making industries. ARBED’s domestic and foreign subsidiaries have interests in steel making and steel products, cement, copper foil production, engineering, and mining. As stated above, mining activity in Luxembourg is very limited and consists of domestic-scale industrial minerals operations. Thus, no specific information could be retrieved on active and inactive mines of the country. 2.3.11 Portugal Portugal has a long history in the exploitation of metallic minerals starting about 2000 B.C. [6]. The first mining operations took place in ‘gossan’ type oxidation zones (for copper, zinc, lead, gold and silver) and gold-bearing placers. Later, the Romans intensively exploited gold and polymetallic sulphide vein deposits [12]. From a geological point of view, Portugal is a considerably diverse and complex country. More specifically, the Iberian Peninsula is one of the most mineralized areas of Western Europe with a very complex geology. Massive sulphides linked to synorogenic vulcanism in the southwestern part of the Iberian Peninsula are well known internationally. The metallogenic province stretches about 250 km from Seville, Spain, to the southwestern coast of Portugal. On that world famous district a total of 30 deposits (11 in Portugal and 19 in Spain), with more than 1120 Mt, were discovered between 1950 and 1998, averaging 1.2 deposits/2 years, which is an amazing exploration performance index. Today, Portugal is a significant European mineral producer and one of Europe’s leading copper producers. It is also a major producer of tin, tungsten, uranium and marble. The Neves-Corvo Mine owned by Somincor and Rio Tinto Ltd. and the Panasqueira tungsten mine of Beralt Tin and Wolfram (Portugal) Ltd. are the two major operations in the metal-mining sector.


45

In Portugal there is no current gold production. However, a number of deposits have been identified and considered to be significant. Jales-Tres Minas is the most important gold district in Portugal while Auspex Minerals Ltd., also announced in 1998 that they discovered 13 deposits with potential economic gold mineralization. Industrial minerals production in Portugal is represented by a variety of materials, most notably ceramics and dimension stone. The dimension stone industry is an important segment of the mining industry in terms of value and trade. Marble is the most valuable of the stone products and accounts for the majority of stone production. The main area for marble mining is the District of Evora. There is a potential for increased production of granite, marble, and slate. In addition, Pirites Alentejanas S.A.R.L. is the country’s largest producer of pyrite. The present structure of the mineral industry could change in the near future because of significant mining exploration by several foreign companies. Copper, gold, kaolin, lead, lithium, pyrites, and tin are some of the minerals targeted for exploration. The Iberian Pyrite Belt is the prime area for exploration activity and appears to have an above-average potential for success on the basis of district’s record of about 90 documented mineralized deposits, an unusually high number of large sulphide deposits. According to the Geological and Mining Institute of Portugal, there are numerous inactive mines in Portugal. 2.3.12 Spain Spain is a significant European producer of non-ferrous precious metals, with some of the most mineralized territories in Western Europe. The main polymetallic deposits, from west to east, include Tharsis, Scotiel, Rio Tinto, and Aznalcollar. There are very few large mines. In terms of value of metallic and non-metallic minerals and quarry products, Spain is a leader among the EU countries. Consequently, Spain has one of the highest levels of self-sufficiency, with respect to mineral raw materials, among the EU members. Of a total of approximately 100 mineral products mined, about 18 are produced in significant quantities, such as bentonite, calcinated magnetite, copper, fluorspar, glauberite, iron, lead, mercury, potassic and sepiolitic salts, pyrites, quartz, refractory argillite, sea and rock salt, tin, tungsten, and zinc [6]. Production of many metallic minerals in Spain is insufficient to meet domestic demand, so these must be imported. For most non-metallic minerals, however, production exceeds by far domestic consumption and the surpluses are exported. The economic development of certain regions, such as the Basque Country and Asturias, is based on their mineral wealth. Therefore, mining is an important current and potential source of income in these areas. Spain is one of the larger coal producers in the EU, with 26 million metric tons per year (Mt/yr) (all types), in 1998. Coal reserves are abundant but difficult to mine. Consequently, cost of production is higher, making Spanish coal less competitive than that of many other countries. The leading producer of soft coal

46 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES is Huelleras del Norte S.A. (Hunosa) and the leading producer of lignite is Empresa Nacional de Electricidad S.A. (Endesa). Copper is mainly mined at the deposits in Sotiel and Migollas in Huelva, by Navan Resources Ltd. (Almagrera) and by Boliden Apirsa at Aznalcollar (Los Frailes deposit) near Seville. Gold was being sought in Asturia, northeastern Spain, by Rio Narcea Gold Mines, Ltd., which acquired concessions and permits that previously belonged to the Spanish subsidiary of Anglo-American Corp. Navan Resources Ltd. inaugurated its new polymetallic (copper, lead, and zinc) Aguas Tenidas Mine near Huelva in November 1997. Aguas Tenidas is the first underground operation to be developed in Spain in several years. The operation supplies Navan’s nearby Almagrera mill and concentrator with 0.8 to 1 Mt/yr of ore. Navan acquired the mill and concentrator, along with three mines, Sotiel, Sotiel Este, and Miggollas, in June 1997. The principal producer of iron ore was Compania Andaluza de Minas S.A. (CAM), which operated its open-pit mine at Marzuesado (Granada). Mining was halted in October 1996, and the mine remains inactive since the end of 1997. However, production started at the nearby Los Frailes, one of the biggest open-pit mines in Europe. Ore production at Los Frailes was estimated to be approximately 4 Mt/yr. Los Frailes was closed in early 1998 after a large toxic spill. A waste reservoir ruptured and sent sludge into a nearby river. The spill poisoned some of the areas around the edges of Donana National Park, Europe’s largest nature reserve. Boliden was undertaking remedial actions and safety requirements in order to restart operations as soon as possible. There are a number of inactive mines in Spain. No specific information could be retrieved on the inactive mines of the country, except that most of them are coal mines. 2.3.13 Sweden Sweden is endowed with significant deposits of iron ore, certain base metals (copper, lead, and zinc) and several industrial minerals, including dolomite, feldspar, granite, ilmenite, kaolin, limestone, marble, quartz and wollastonite. The country is well known for the production of high-quality steel. Sweden has developed nuclear and hydroelectric power, since the country must rely heavily on hydrocarbon imports owing to inadequate indigenous resources. After acceding to the EU on 1 January 1995, Sweden liberalized its mineral policy to parallel EU standards. The policy, based on the Swedish Minerals Act, 1992, eliminated laws requiring foreign companies to get special permission for prospecting, annulled the state’s participation in mining enterprises (so-called ‘crown shares’) and revoked all taxes and royalties, except for a 28% corporate tax, one of the lowest in Europe. Furthermore, an exploration permit holder cannot receive an exploration permit until adequate financial and technical capabilities can be proven [6]. The two largest companies in Sweden are Boliden AB, owned by Boliden Ltd, and the government owned Luossavaara-Kiirunavaara AB (LKAB).


47

Laisvall is the largest lead mine in Europe and it is located in Arjeplog Municipality, in northern Sweden, towards the Norwegian border. In January 1999, total proven and probable reserves were 6.8 Mt grading 0.8% zinc, 4.6% lead and 11 g/t silver. Measured and indicated reserves at that time were 3.35 Mt grading 1.2% zinc, 2.0% lead and 9 g/t silver. The company has planned to increase the ore output rate from Laisvall to 2.2 Mt/yr, given regulatory approvals [13]. Located near Hedemora, in the historic Bergslagen mining district of central Sweden, the two mines and common concentrator at Garpenberg comprise the smallest of Boliden’s mining areas. The company bought the Garpenberg mine and mill from AB Zinkgruvor in 1957. The exploration of a silver-rich area to the north during the 1960s led to the development of a second mine, Garpenberg Norra (Garpenberg North). The open-pit Bjorgdal mine is the largest gold mine in Western Europe. The former owner, Terra Mining AB, was bought by Williams Resources Inc. in 1996. Williams Resources was continuing exploration activities and reported in 1998 that it had increased estimated minable reserves to 8.6 Mt of ore grading an average of 2.32 g/metric ton gold [14]. LKAB has iron ore mines and processing plants in Kiruna and Malmberget, a pelletizing plant in Svappavaara, and harbors at Luleå and Narvik. The company operated close to full capacity in 1997. LKAB’s Malmberget (ore mountain) iron ore mine, located at Gällivare, 75 km from Kiruna, contains some 20 orebodies spread over an underground area of about 5 by 2.5 km. Seven are currently being exploited. Mining began in 1892 and since then over 350 Mt of ore have been produced. Kiruna has the world’s largest underground iron ore mine. The orebody in Kiruna is an enormous slice of magnetite. It is about four kilometres long, has an average width of 80 m and extends to an estimated depth of around 2 km at an incline of roughly 60°. The main haulage level is at a depth of 1.045 m. Mining of the orebody between levels 1.045 and 775 will continue until about the year 2018. Up to now, about 940 million tons of ore have been extracted from the Kiruna orebody. The Zinkgruvan Mine, the largest zinc mine in Sweden, is owned by North Mining Svenska AB, a subsidiary of the Australian company, North Limited. Underground mining started in 1857. In the early 1990s, new technology and careful management reduced mining and milling costs to about 50%, converting a high-cost operation to the sixth lowest-cost zinc producer in the Western World by 1993. Currently, the operation is producing about 700,000 t/yr of zinc in concentrate. The total production of industrial minerals, except aggregates and dimensional stones, in 1997 reached 9 million tons, a level that has been fairly constant during the 1990s. Limestone products, including dolomite and limestone for cement production, form 90% of the total, while silica sands, quartzite, feldspar, olivine and talc make up for the remaining 10% of the output. Tricorona Mineral AB owns three major mineral deposits, namely graphite, kaolin and wollastonite, of which only the graphite was in production in 1998. Three subsidiaries were formed to handle the development of the deposits, Woxna Graphite AB, Svenska Kaolin AB and Aros Mineral AB respectively [15].

48 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES According to the Swedish authorities on underground exploitation, the total number of abandoned mines is 25 in Northern Sweden and 775 in Central and Southern Sweden. 2.3.14 The Netherlands In terms of world production, the Netherlands is a modest producer of metallic and non-metallic minerals and mineral products. Production of mineral commodities generally remained the same or dropped slightly in 1998, compared to previous years. The high cost of social benefits contributed to the production costs of Dutch products making them less competitive on the world market. The only mining operations left in the Netherlands are the extraction of peat, salt, and sand and gravel. The metal-processing sector relies almost exclusively on imported raw materials [6]. The Netherlands has no commercially exploitable reserves of metal ores. The only active mines that exist in the country extract industrial minerals. No specific information could be retrieved on inactive mines of the country. 2.3.15 The United Kingdom Mine production of ferrous and non-ferrous metals in the UK has been declining for the past 20 years as reserves become depleted. Since processing is the basis of a large and economically important mineral industry, significant imports are required to satisfy metallurgical requirements [6]. Operations in the steel sector showed moderate increases as the demand for steel increased. The industrial minerals sector has provided a significant base for expanding the extractive industries, and the balance has shifted away from the metallic mineral sector. Companies had a substantial interest in the production of domestic and foreign industrial minerals, such as aggregates, ball clay, gypsum, and kaolin (china clay). Production of iron ore is limited to a small amount of hematite ore, mined by Egremont Mining Co. at the Florence Mine in Cumbria. The output goes for pigments and foundry annealing uses, rather than metal production. Primary steel production is based on imported iron ore, mainly from Australia and Brazil. Activities in gold exploration and development in the UK increased in 1998. Northern Ireland, Scotland, and Wales continued to be the three main areas of exploration by companies. Scotland was the most active area with several exploration licenses in effect. The UK is the leading world producer and exporter of ball clay, as well as the world’s largest exporter and second largest producer, after USA, of kaolin (china clay). Watts, Blake, Bearne & Co. Plc. (WBB) is the country’s largest producer of ball clay. WBB Devon Clays Ltd. is responsible for the ball clay operations of WBB. The division operates eight open-pits and three underground mines that have a total combined capacity of 500,000 t/yr of crude ball clay.


49

English China Clays Plc. (ECC) is the largest producer of kaolin and one of the major producers worldwide. Operations are mainly found in the southwestern area of the UK. ECC Ball Clays Ltd. is responsible for the domestic ball clay operations of ECC. The division operates five quarries and three underground mines that have a combined output of 450,000 t/yr of crude ball clay. ECC International Ltd. operates ball clay and kaolin mines and quarries in the Wareham Basin, Dorsetshire; the Bovey Basin, South Devonshire; and the Petrockstowe Basin, North Devonshire. The majority of the production comes from the Bovey Basin. Fluorspar mining is concentrated in Derbyshire, from the Southern Pennine deposit. The major producer is Laporte Industries Plc., which operates two underground mines and one open-pit mine. The ore is processed at Laporte’s Cavendish Mill near Sheffield. Durham Industrial Minerals Ltd. was to close five fluorspar mines at Rookhope in Weardale. Falling prices of fluorspar, Chinese competition, and the strength of the pound were thought to have contributed to the closings [16]. British Gypsum Ltd., a subsidiary of BPB Industries Plc., is the major producer of gypsum in the UK. The company has mines in Cumbria, Leicestershire, Nottinghamshire, Staffordshire and Sussex that produce about 3 Mt/yr of gypsum. With few exceptions, this material supplies the domestic market. Cleveland Potash Ltd. (CPL), the only potash producer in the UK, operates the Boulby Mine in Yorkshire. CPL also mines rock salt as a co-product from an underlying seam in the Boulby Mine. Boulby potash occurs at depths between 1200 and 1500 m in a seam ranging from 0 to 20 m but averaging 7 m in thickness [17]. Most slate mining in the UK occurs in northern Wales; additional mining operations are found in Cornwall and the Lake District. Alfred McAlpine Slate Ltd. is the owner and operator of the Cwt y Bugail, Ffestiniog, and Penrhyn quarries in North Wales. The Penrhyn quarry at Bethesda, measuring 2.415 by 805 m, is considered to be the world’s largest slate quarry and has been in operation for more than 400 years. The company also produces natural slate from its American quarry at Hilltop Slate Inc., New York. Historically, natural slate has been used in roofing applications, but in more recent times, markets have been extended to include interior flooring and windowsills together with ornamental landscapes. McAlpine Slate produces more than one-half of the UK’s entire production of natural slate. The company exports about two-thirds of its production, mostly to Europe. McAlpine received planning permission to exploit additional reserves at its Penrhyn quarry. The quarry, which covers an area of about 325 hectares (h), will be extended by an additional 45 h. This enlargement will extend the life of the quarry and increase extraction by a further 80 million metric tons of slate at the southern end of the quarry [18]. RJB Mining Plc., the largest coal mining company in the UK and the largest independent coal producer in the EU owns most of the coal mining industry. The largest operation is the underground Selby Complex, consisting of Riccall/ Whitmoor, Stillingfleet Combine and Wistow. There were also 24 small drift mines in operation in 1998. Open-pit mines in production in 1998 totalled 83. RJB Mining owned 16 producing open-pit mines; Celtic Energy Ltd. owned 5 open-pit

50 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES mines; and Scottish Coal Company Ltd. had 11 open-pit mines in Scotland. The remaining open-pit mines were operated by more than 25 other operators. The UK has been a significant player in the world mining and mineralprocessing industries. This has been more the result of an extensive range of companies in the country, with various interests in the international mineral industry rather than the domestic mineral industry. This scenario is expected to continue. Exploration is expected to continue onshore and offshore. Onshore exploration activities will be directed mainly toward precious metals. Offshore exploration interest will continue to be focused on North Sea areas, particularly the areas west of the Shetland Islands, the Central North Sea, and the Southern Gas. Five large underground mines in the UK ceased operations in the period 1998–2000.

2.4 Inactive underground mines used as waste disposal sites Although the storage of wastes in inactive underground mines has attracted considerable interest in the past twenty years, it could be considered as a fairly recent concept. Salt mines, which usually are excavated by the room and pillar method, are of great interest in view of the possibility of reusing the openings for waste disposal. Some examples of inactive underground mines that have been used as waste repositories are shown in Table 2.4. Several studies have been conducted on the feasibility of a deep geological disposal site and various geological media have been analysed for their thermal, mechanical and chemical properties. As a result, four underground research laboratories are currently in operation in Europe: crystalline granite is being investigated at Grimsel (Switzerland) and Stripa (Sweden); the suitability of clay analysed at Mol (Belgium) and a salt formation is being studied at Asse (Germany). Furthermore, laboratories are scheduled for the near future or are already under construction, namely in France, Sweden (Aspo) and the UK (Sellafield). It must be specified that both Stripa and Asse are inactive underground mines [20]. Major past or present underground research laboratories are shown in Table 2.5. The information below is a brief description about underground inactive mines that have been used as waste repositories, underground laboratories and for research purposes related with storage of wastes. 2.4.1 Morsleben salt mine Morsleben repository is located in the federal state of Saxony-Anhalt [22]. At the site, potassium was mined until the early twenties. Thereafter, rock salt mining went on until 1969. Both the above operations left open cavities with a volume of approximately 10 million m3. In 1970 the nuclear power plant operator of the former German Democratic Republic bought the mine to convert it into a low-level (LLW) and intermediatelevel waste (ILW) repository. After a licensing procedure, waste disposal started in 1978 using rock cavities below the 500 m horizon for waste emplacement.

Table 2.4: Examples of inactive underground mines that have been reused as waste repositories in Europe [19]. Name of mine Germany

Type of ore

Type of reuse

Notes

Bartensleben mine Konrad mine Heilbroun mine

Salt Iron Salt

Kochendorf salt mine

Salt

Walsum mine

Coal

Haus Aden/Monopol mine

Coal

Zielitz mine Morsleben mine

Potash Salt

Herfa-Neurode mine

Salt

Storage of radioactive wastes Storage of radioactive wastes (under study) Storage of fly ash wastes; storage of anhydrite and clay contaminated with Hg Storage of flue gas, desulphurization residue from incineration plants and siliceous slags (under study) Storage of fly ash from incineration plants in the goaf (under study) Storage of fly ash from incineration plants in the goaf (under study) Storage of industrial wastes Storage of radioactive wastes and sealed radiation sources Storage of hazardous wastes

France

Joseph-Else mine

Potash

Storage of industrial wastes (under study)

Room and pillar

Italy

Codana mine Besta mine

Gypsum Dolomite

Storage of industrial wastes Storage of inert debris (36.000 m3 reused)

Room and pillar Room and pillar

Russia

Verkhnekamsoye area mines

Potash

Storage of waste

Room and pillar

Slovenia

Velenje mine

Coal

Storage of fly ash (under construction)

Longwall mining

UK

Walsall Wood colliery old mine Dudley mines

Coal Limestone

Geostow project

Salt

Storage of chemical wastes (since 1965) Colliery waste and fly ash pumped in the voids from the surface Storage of fly ash from incineration plants

Room and pillar Room and pillar Longwall mining

Room and pillar Room and pillar

Room and pillar


Longwall mining

51

52 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 2.5: Major past or present underground research laboratories [21]. Rock formation Salt

Crystalline rock

Argillaceous rock

(bedded) (dome) (dome) (bedded) (dome) (granite) (granite) (granite) (granite) (granite) (granite) (granite) (granite) (granite) (granite) (basalt) (plastic clay) (clay-marl)

Laboratory name

Country

Salt Vault (Kansas) Avery Island (Louisiana) Asse WIPP (New Mexico) Hope Stripa Grimsel Edgar mine (Colorado) Tono mine URL (Manitoba) Climax mine (Nevada) Fanay Augeres Akenobe mine Hard Rock Laboratory NSTF (Washington) G-tunnel (Nevada) Mol Pasquasia

USA USA Germany USA Germany Sweden Switzerland USA Japan Canada USA France Japan Sweden USA USA Belgium Italy

Morsleben became a Federal Facility following German reunification, DBE was then contracted to operate the site. In this deep geological repository different categories of solid LLW and ILW as well as sealed radiation sources are disposed of. Essentially, LLW packed in drums is stacked in chambers, while waste with higher activity content, delivered to the repository in shielding overpacks, is discharged through shielding lock systems into closed chambers below a drift. Waste disposal (Fig. 2.2) is carried out on the basis of contractual arrangements between waste producers and the Federal Government. Ownership of the waste is passed over upon delivery; the producers pay a fee that settles for all costs. In 1998, the radioactive waste disposed at Morsleben amounted to 36.752 m3 radioactive waste and 6.621 sealed radiation sources. 2.4.2 Herfa-Neurode salt mine The Herfa-Neurode underground waste repository (Figs 2.3–2.5) is owned by Kali und Salz Entsorgung GmbH, which also operates another underground waste repository named Zielilz [23]. Hazardous waste disposal has been undertaken there for the last 30 years. The underground waste disposal plant is located in a mining concession of the potash mine Winterschall at Heringen/Were in Germany. The mine is situated in a 300 m thick salt formation, covered by clay


Figure 2.2: Waste disposal at Morsleben.

Figure 2.3: Surface view of the Herfa-Neurode repository.

53


Figure 2.4: Underground view of the Herfa-Neurode repository.

Figure 2.5: Underground view of the Herfa-Neurode repository.


55

layers, at a depth of about 800 m. Due to the clay layer, the salt deposit is isolated against the covering aquiferous layer and has therefore remained almost unchanged for the past 240 million years. During the extraction of the potash deposits extending over an area of 1200 km2, cavities were formed using the room and pillar mining method, which are now used for the disposal of hazardous waste materials. The underground waste disposal plant was admitted in accordance with waste law. The supervisory authority is the Mining Authority, Hessen. In addition to the Waste Act, mining regulations are also involved as far as the operation of the plant is concerned. The capacity of the plant depends, practically, on the haulage capacity in the Herfa shaft, which has a payload of 7 tons. The annual capacity of the haulage plant is 200,000 tons. The underground cavities permitted by the mining authority for hazardous waste storage are sufficient for 20 more years. The 30% of the waste currently stored come from the local area of Hessen, 50% from other Federal Lands and 20% from foreign countries of Western Europe. The classification of the waste origin, and its percentage share of the total, is as follows: • • • • •

residues from the flue gas cleaning of incinerator plants: 30%; building rubble and earth excavation from demolition and renovation: 25%; metal-processing industry: 20%; residues from the chemical industry: 20%; electrical industry (transformers, capacitors): 5%.

The waste is put together into material groups. Within a material group, wastes which have similar substances are stored together. 2.4.3 Konrad iron mine Iron ore mining started in the former Konrad mine (Fig. 2.6) in Lower Saxony in the sixties and was phased out for economical reasons in 1976 [22]. At the same year the Konrad site was selected for investigation as a possible repository because of the great depth of the ore horizon, the fact that the mine is extraordinarily dry and the complete isolation from shallow groundwater by clayish overlying rock. Results of an extensive survey and evaluation programme led in 1982 to a positive statement regarding the site’s suitability to host a radioactive waste repository. DBE has developed the repository technology, carried out the licensing procedure in cooperation with the government and will later transform the mine into a repository and operate it. According to the license application, Konrad will be a repository for waste with negligible decay heat. Approximately 90% of the waste volume arising in Germany belongs to this category. The Konrad repository will consist of 6 emplacement fields at different levels between 800 and 1300 m depth. A net disposal capacity of approximately 650,000 m3 of waste packages will be available. Fig. 2.7 shows a scheme of planned mine operation.


Figure 2.6: The Konrad mine [24].

Figure 2.7: Scheme of planned mine operation [24].


57

2.4.4 Stripa iron mine Mining of Stripa iron mine (Fig. 2.8) dates back to the 15th century. During long periods of time mining occurred only sporadically, with a complete standstill between 1634 and 1771 [25]. Mining ceased in 1976 with a total production of 18 million tons of crude ore – quartz banded hematite. The mining operation ceased because the whole orebody had been mined. Between 1977 and 1980 a common Swedish-American project (SAC, Swedish American Cooperation) was carried through in Stripa. The project consisted of three main parts: • heat experiments with simulated waste containers; • evaluation of fissure hydrology; • geophysical measurements. Extensive information was obtained about mechanical reactions to heat in the control and ground water current in fissures in crystalline rock. The Swedish – American

Figure 2.8: Stripa mine [26].

58 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Cooperation project attracted international interest and the international Stripa Project began in 1980. The research work was carried out as an independent project in the OECD Nuclear Energy Agency (NEA). Participating countries were: Finland, France, Japan, Canada, Great Britain, Spain, Switzerland, Sweden, and USA. The research was divided into the following areas: • detection and mapping of fissure zones; • groundwater conditions and nuclide migration; • examination of bentonite clay for refilling and stopping up. This part of the research went on up to the end of 1985. A third phase in the research began in 1986 and went on up to 1991. All previously mentioned countries except France and Spain participated in this part. The major aim of the third phase was research about: • • • •

hydrogeology, chemical transportation, engineering barriers, geophysics.

2.4.5 Asse salt mine Asse salt mine was used as a research laboratory for evaluation purposes (Fig. 2.9) of the salt disposal concept of Germany. The exploitation method used was room and pillar. The depth varies between 490 and 830 m. In 1965, the ownership of the Asse salt mine was transferred to GSF for the purposes of carrying out research

Figure 2.9: Storage of wastes in Asse mine for research purposes [27].


59

into the safe ultimate disposal of radioactive wastes. Since 1967, LLWs have been emplaced for experimental purposes until 1993, when experiments for the ultimate disposal of radioactive wastes at the Asse mine stopped. Finally, it should be noted that there are also other underground mines that have been used as waste repositories, as shown in Table 2.4, but no detailed information about their operation is available. For example, chemical wastes have been stored in England since 1965 in an old mine at Walsall Wood colliery, at a depth of about 900 m. The mine is isolated environmentally by a geological graben with clay-filled faults on both sides and shale above.

References [1] Kaliampakos, D. & Menegaki, M., Hazardous waste repositories in underground mines. A possible solution to an ever-pressing problem. Proc. of the 1st Conf. On Sustainable Development & Management of the Subsurface, Utrecht: Netherlands, 5–7 November 2003. [2] Carmody, J. & Sterling, R., Underground Space Design: A Guide to Subsurface Utilization and Design for People in Underground Spaces, Van Nostrand Reinhold: New York, 1993. [3] Kaliampakos, D., Mavropoulos, A. & Damigos D., Reducing risk of exposure from hazardous waste repositories, presented at the Environmental Health 2003 Conference, Catania, Italy, 2003. [4] Kaliampakos, D., Mavropoulos, A. & Prousiotis, J., Abandoned mines as hazardous waste repositories in Europe. Proc. of the 18th Int. Conf. On Solid Waste Technology and Management, Philadelphia, PA, 23–26 March 2003. [5] National Technical University of Athens (NTUA), Survey of underground mines in Europe. Low Risk Disposal Technology Research project (Ε.Ε. EVGI-CT-2000-00020), Deliverable D1.1, 2000. [6] United States Geological Survey (USGS), Minerals Information – Europe and Central Eurasia, 2001, URL: http://minerals.usgs.gov/minerals/pubs/ country/europe.html [7] Knudsen, C., Nordic minerals review – Denmark, Industrial Minerals, No 374, pp. 52–55, November, 1998. [8] Nurmi, A.P. & Peter, S.-W., Mining and Exploration in Finland, Society for Geology Applied to Mineral Deposits, News, No. 2, November 1996. [9] Industrial Minerals, France – What next after MDPA has gone?. Industrial Minerals, No. 367, p. 54, April 1998. [10] Mining and Metals, Tapping into Greece’s mineral treasure chest, February 1998, URL http://www.ana.gr/hermes/1998/feb/mining.htm [11] Sol, M.V., Peters, S.W.M. & Aiking, H., Toxic Waste Storage Sites in EU Countries, A Preliminary Risk Inventory, IVM Report number: R-99/04, February 1999. [12] Geological and Mining Institute of Portugal, 2001. [13] Mining Technology, 2000, URL: http://www.mining-technology.com

60 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES [14] Coal age, Bjorkdal gold mine is Europe’s largest, Coal Age, 103(3), p. 38, March 1998. [15] Beckius, K. & Thomaeus, M., Nordic review – a series of features highlighting the industrial minerals of Nordic countries. Sweden, Industrial Minerals, No. 374, pp. 52–82, November 1998. [16] Industrial Minerals, Durham fluorspar mine closures imminent, Industrial Minerals, No. 373, p. 15, October 1998. [17] Pearson, K., Potash producers. Industrial Minerals, No. 367, p. 57, April 1998. [18] Industrial Minerals, McAlpine to extend Penrhyn slate quarry, Industrial Minerals, No. 365, p. 30, February 1998. [19] Peila, D. & Pelizza, S., Civil reuses of underground mine openings: a summary of international experience. Tunnelling and Underground Space Technology, 10(2), pp. 179–191, 1995. [20] Decamps, F. & Dujacquier, L., Overview of European practices and facilities for waste management and disposal. Nuclear Engineering and Design, Elsevier Science S.A., 176, pp. 1–7, 1997. [21] International Association for Nuclear Energy, 2001, http://www. uilondon.org [22] DBE mbH, 2000, URL: http://www.dbe.de [23] Kali und Salz, URL: http://www.kalisalz.basf.de [24] Bfs, The Konrad Repository Project, From an Iron Mine to a Repository for Radioactive Wastes, Salzgitter, 1994. [25] Stripa Mine Service AB, 1999, http://www.stripa.se [26] Lawrence Berkeley National Laboratory, 1997, http://imglib.lbl.gov [27] National Research Center for Environment and Health, 2000, http://www. gsf.de/Wir_ueber_uns/index_en.phtml

CHAPTER 3 Criteria for selecting repository mines R. Pusch

GeoDevelopment AB, Lund, Sweden.

Abstract This chapter discusses the most important criterion for selecting repository mines. The ideal mine to be converted to a safe waste repository is a rather small, modern, remotely and relatively deeply located, mine with intact power supply, pump systems and ventilation. The geological host medium is very important. Crystalline rock has excellent stability of the drifts and rooms even at large depths but it has a relatively high hydraulic conductivity. Salt contains no free water and offers very good isolation of the waste, but brine in local sediment lenses may cause difficulties in the preparation of the mine for waste application. Argillaceous rock has a very low hydraulic conductivity but poor stability and the vicinity of the drifts may be very conductive. The chapter gives examples of deep abandoned mines in granite, i.e. the Stripa mine in Sweden, formerly used for exploitation of iron ore, and of mined rooms in a salt dome as well as in limestone. They are taken as a basis of calculations of the mechanical stability, evolution of engineered barriers, and migration of released toxic elements to an imaginary well located close to the waste-filled rooms.

3.1 Introduction The most important criterion for selecting repository mines is that the host rock should be low-permeable and mechanically stable, and that the mines should have suitable drifts and rooms for placement of waste packages. The ideal mine to be converted to a safe waste repository is a rather small, modern, remotely and relatively deeply located mine with intact power supply, pump systems and ventilation. The geological host medium is very important. Crystalline rock has excellent stability of the drifts and rooms even at large depths but it has a relatively high

62 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES hydraulic conductivity. The creep potential is very low and self-sealing and hence unimportant. Salt contains no free water and offers very good isolation of the waste, but brine in local sediment lenses may cause difficulties in the preparation of the mine for waste application. The creep potential is very high which means that the drifts and rooms converge and self-seal. Argillaceous rock has a very low hydraulic conductivity but poor stability and the vicinity of the drifts, i.e. the excavation-disturbed zone (EDZ), may be very conductive. It can undergo substantial creep and can self-seal depending on the diagenesis. Limestone rock has a low stability and is pervious. It has some creep and self-sealing potentials. Its most valuable property is the high pH of the porewater. Mines in several other types of geological media, like metamorphous rock, shales and marble, can be considered for waste disposal but they are regarded here as representatives of the four types mentioned above. Thus, gneiss, shales and marble in principle behave like granite or argillaceous rock.

3.2 Rock structure The structural constitution of the rock mass in which the mine is located determines the rate and distribution of the groundwater flow through the mine to the surroundings and hence the transport to the biosphere of toxic elements that can be released from the waste. For comparison and forming a basis for flow calculations it is necessary to work out relevant generalized rock structure models. The transmissivity of the host rock determines its isolating capacity and is therefore the most important factor for the long-term function of the mine. It is controlled by the rock structure, which is hence a primary factor for the performance. It is also a determinant of the mechanical stability of the mine. The scheme in Table 3.1 is applicable to most rock types except salt. 3.2.1 Crystalline rock Many granites can be represented by a generalized orthogonal-type rock structure model like the one shown in Fig. 3.1, which includes practically important discontinuities of different orders. Metamorphic rock like gneiss commonly has a more wavy macroscopic nature and more anisotropic structural organization but it can still be represented by the same model except that the spacing of sixth- to fourth-order discontinuities is usually much smaller in one direction than in the two other. We will consider a deeply located underground research laboratory in Sweden, extending from a former iron ore mine in Sweden, as the reference case (Stripa mine) [2]. 3.2.2 Argillaceous rock Mines in argillaceous rock are common in many countries, the exploitable ore often being impregnations of lead, copper and a number of other metals (Fig. 3.2).

Table 3.1: Categorization scheme for rock structure with typical geometrical, hydraulic and strength data [1, 2]. (The crystal matrix has typically K < 10–13 m/s.) Discontinuity

General properties

Length

Hydraulic conductivity (K) (m/s)

Hundreds

10–7–10–5

Tens to hundreds

10–8–10–6

Metres to tens of metres

10–10–10–7

High-order discontinuities (conductivity refers to rock with no discontinuities of lower order) Fourth order Discrete major fractures, water-bearing, Tens of metres little or no gouge, strong Fifth order Little water, no gouge, high strength Metres Sixth order Decimetres, no water, no gouge, very Decimetres high strength Seventh order Centimetres and smaller (fissures, voids) Centimetres and smaller

–

10–11–10–9

– –

10–12–10–10 10–13–10–11

–

Kilometres very low strength Second order Major fracture zones, water-bearing, Kilometres gouge, low strength Third order Minor fracture zones, water-bearing, Hundreds some gouge, relatively strong of metres

Width (m)

63


Figure 3.1: Typical appearance of crystalline rock. The breaks represent thirdand fourth-order discontinuities while the finer weaknesses represent fifth- and higher-order discontinuities.

Figure 3.2: Formation of ore (black) in sedimentary rock due to impregnation by solutions.

The figure is typical in the sense that the mode of formation, i.e. deposition and consolidation of sediments, has often resulted in very strong variation in composition and geotechnical properties. Argillaceous rock can be considered as a less brittle version of metamorphic rock and can also be represented by Fig. 3.1 although with even smaller spacing of the discontinuities in one plane (direction), and hence significant anisotropy.

CRITERIA FOR SELECTING REPOSITORY MINES

65

Comprehensive experience from exploration of such rock in France and Switzerland has shown that low-order discontinuities are less conductive than in crystalline rock because tectonically induced shearing has led to disintegration and significant sealing. The rock matrix, i.e. the rock between the low-order discontinuities, has a hydraulic conductivity and a transmissivity as low as those of crystalline rock or somewhat lower. Drifts and tunnel systems in northern Switzerland serve as typical representatives of rooms for disposal of hazardous waste in sedimentary rock. Such rooms are presently used as underground research laboratories for development of techniques for disposal of highly radioactive waste (Mont Terri), [3]. 3.2.3 Salt rock Rock in the form of domal salt – usually of sodium or potassium type – or bedded salt is very suitable for waste disposal except if it contains brine pockets. It is already being utilized in many countries like Germany and France because completely homogeneous salt is perfectly tight with respect to water and gas. A necessary prerequisite is to construct long-lasting seals in the form of plugs in the shafts leading down to the repository level since water inflow from shallow soil and rock can cause very difficult problems. Salt mining has been made at all levels but only mines located several hundred metres below the ground surface should be considered. Figure 3.3 is a schematic drawing of a salt dome, surrounded by other rock that caused salt in an underlying salt bed to be squeezed up to form the dome. The process forced up material from the surroundings yielding internal flow structures and irregularly spaced and oriented lenses of clay/silt/sand, which represent inclusions of brine. All these discontinuities affect the stability of rooms in the salt rock and can contain brine. The figure also shows a cross section of the Asse salt mine that has been used as an underground research laboratory by the Gesellschaft fuer Anlagen- und Reaktorsicherheit GmbH (GRS) in the last decades [3]. It may well be used for disposal of hazardous chemical waste. The spacing of major discontinuities varies with the size of the salt domes and for the Asse case it is assumed to be 50–100 m within 200 m distance from the boundary of the dome and 100–200 m in the interior. They do not intersect, and hence the only connection with the biosphere is where the rooms are intersected by lenses that extend all the way up the ground surface. The lognormal persistence of the lenses is assumed to vary between 100 and 1000 m, the shorter ones being termed here thirdorder discontinuities and the longer ones second-order discontinuities. Despite the excellent isolating potential of salt caused by the absence of free water, there are two not solved problems yet: (1) gas production in the waste saturated with brine can cause extremely high pressures that may lead to upward penetration of gas and expulsion of heavily contaminated brines; (2) the very significant creep properties of salt rock will make retrieval of waste packages impossible after some 50–100 years since heavy objects sink in an unforeseeable


Figure 3.3: Structural nature of a salt domes. Top: Generalized rock structural model. Bottom: The Asse salt mine [3].


67

way in the salt mass. For these reasons disposal in salt cannot be proposed as a first choice method. 3.2.4 Other rock types In certain countries mining has been extensive in very porous rock like limestone and abandoned mines in such geological media may be the only alternative. Mines located in regularly bedded limestone as well as heterogeneous limestone like ancient coral reefs, may have to be considered as options for disposal of hazardous waste. The hydraulic conductivity and transmissivity may be very high and the mechanical stability very low, which is of course not suitable. However, the high pH of the groundwater provides good chemical conditions for minimizing dissolution of various types of waste. The permeable nature of many limestone regions requires construction of very effective engineered barriers. We will use a bauxite mine in limestone environment in Greece as a reference in later chapters dealing with stability and waste isolation efficiency.

3.3 Requirements for the use of mines as repositories 3.3.1 Function of the host rock A major criterion for use of abandoned mines as waste repositories is that elements released from the waste must not contaminate groundwater in the mine area more than what is accepted by regulatory authorities. The geological medium must provide mechanical protection of the ‘chemical apparatus’, i.e. the backfilled rooms with waste embedded in and surrounded by engineered barrier systems (EBS), and yield slow release of toxic elements to the biosphere. The processes that can threaten and degrade the geological medium hosting the repository mine are tectonic events, glaciation involving deep abrasion and erosion, and loss of sealing ability of the engineered barriers. The capacity of mine repositories to isolate waste is determined by: 1. The physical stability of the rock and the physical and chemical performance as well as the stability of the EBS. 2. The rock structure and related hydraulic conductivity and the conductivity of the EBS are key factors for the performance of mine repositories. 3. The impact of groundwater chemistry on the longevity of the EBS, and the chemical nature of dissolved hazardous waste elements released from the EBS are key factors. 3.3.2 Conversion of mines to repositories The major issues are the location of the mine with respect to the risk of contaminating drinking water in the closest wells, the status of the mine with respect to the mechanical stability and the cost for converting it into a repository. The most

68 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES important parameters in addition to the issue of groundwater contamination are: • • • • • • •

size, remaining exploitable ore, rock structure, hydrology, and stability, transport to and in the mine, technical facilities, stabilization, cost.

3.3.3 Size Mines that can be considered for disposal of toxic chemical waste are those with relatively large underground space suitable for storing the waste, 5000 m3 being a practical minimum. Drifts for disposal should have a geometry that is suitable for rational application of waste packages. Horse-shoe or rectangular cross section shape of drifts and rooms with 5–30 m height and width and a length of 50–200 m are preferable. Big rooms may require significant stabilization and sealing of the rock. 3.3.4 Remaining exploitable ore The reasons for abandoning a mine is commonly that practically all the ore has been mined out or that continued extraction of ore gives too little profit. However, in the second case, future methods for extracting and refining valuable minerals may make such mines interesting again. Thus, careful analysis has to be made of what the possibilities are to continue mining operations. Metal ore may be of quite different economic value today and in a few tens of years from now, of which uranium, titanium, gold and platinum are historical examples. It is much less significant for iron ore mines, which therefore represent attractive alternatives. Other mines of considerable interest are those in which clay minerals have been mined. An attractive principle in selecting mines for disposal of chemical waste is to use mines in which the exploited ore contained the same types of hazardous elements as the waste. Thus, mines in sulphide ore districts where mercury, arsenic, and lead have impregnated the rock and contaminated the groundwater are suitable for disposal of waste containing these elements. One can also include abandoned, deeply located railway and road tunnels in the group of fully exploited mines. Examples are certain road tunnels in the Alps region located kilometres below the ground surface. 3.3.5 Rock structure, hydrology, and stability 3.3.5.1 General The suitability of an ore mine to be used for waste disposal depends primarily on the risk of contamination of the groundwater, especially water for drinking


69

purposes and irrigation. Most rocks are permeable because of the presence of natural fractures and systems of fracture zones, which determine the transport of contaminants and make certain host rocks less suitable. An important fact is that the drifts and mined-out rooms are surrounded by an excavation-disturbed zone (EDZ) with reduced mechanical stability and increased hydraulic conductivity. Where the EDZ interacts with natural strongly water-bearing fracture zones there are conditions for poor stability and quick and extensive transport of contaminants to the biosphere. This is the reason why all waste disposed in any underground repository must be effectively isolated by engineered barrier systems. The transmissivity of a rock mass is much higher when the frequency of waterbearing discontinuities is high than if the spacing of such features is low and their interconnectivity poor. Even the first mentioned type of rock can be used successfully for safe waste disposal but more effort and money have to be spent on the engineered barriers than in the latter case. Hence, stable and lowpermeable rock is preferable. It is desirable to select mines with neutral or slightly alkaline ground-water because it minimizes the solubility of heavy metals and enhances the longevity of cement- and clay-based engineered barriers provided that pH is not too high. 3.3.5.2 Rock structure modelling Rock structure is a key issue since reliable calculation of the transport of chemical elements released from the waste requires that a representative rock structure model can be defined and used. The matter has been considered in several practical hydropower projects and comprehensive research programmes related to the disposal of radioactive waste. In this book we will show how rock structure models can be used for both rock mechanical and hydrological calculations. The basis is the rock categorization scheme in Table 3.2, which is a simplified version of Table 3.1. Figure 3.4 shows a generalized structural model. Table 3.2: Generalized scheme of rock discontinuities [1]. First to third are fracture zones, fourth to seventh are discrete fractures. Order First Second Third Fourth Fifth Sixth Seventh

Length

Hydraulic conductivity

>Kilometres Kilometres Hundreds of metres Tens of metres Metres Decimetres L f ,

(6.8)

k f >> km ,

where wf is the local aperture of the fracture and Lf is the extension of the fracture. Therefore, it is possible to represent the solution in the fracture as a superposition of the 2D solution on the tangential plane and the 1D profile f(z) along z′ h ( x, y , z ) = h f ( x ′, y ′ ) ,

0 ≤ z′ ≤ wf .

(6.9)

164 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Porous Block A

nm

D

P2

P3

P1

np

nf

Fracture Plane

Γ nm

Pipe

B

C

Figure 6.1: Intersection of two fractures.

Integration of (6.7) along z' yields − k f w f ∇22D h f =

∑v

m ,i ,

(6.10)

i = A,B

where ∇2D := ∇(...) − ∇( ) ⋅ z ′.

(6.11)

The indices A and B stand for the two blocks of porous matrix adjacent to the fracture. vm is the velocity in the porous matrix boundary that limits with the fracture pointing parallel to its outward normal nm (see Fig. 6.1); and wf is the equivalent aperture of the fracture. wf

wf =

∫ f ( z ') dz ′ =: w

f

(1 + β) .

(6.12)

0

6.2.1.4 Fracture intersections In any arbitrary interconnected fracture network, a certain number (mf) of fractures might intercept each other converging into a common channel. The resulting channel might have material properties significantly different from its adjacent environment (either fractures or porous matrix), in the same way that fractures represent a discontinuity for the adjacent blocks of porous matrix. Furthermore, regarding that single fractures are represented by surfaces, it is natural to represent their intersections by 1D curves in the 3D space. In the fracture intersections or pipes (the theoretical representation of the real fracture intersections or channels), integration of the continuity equation over the cross section Ap (see Fig. 6.1.) yields:

∫

Ap

−k p

∂ 2 hp dA = v fn dΓ , ∂η 2

∫ “

(6.13)

RISK ASSESSMENT OF UNDERGROUND REPOSITORIES

165

where v fn = − k

∂h f ∂n f

(6.14)

is the velocity along the fracture planes adjacent to the pipe in the direction of the outward-to-the-fracture normal unitary vector perpendicular to the longitudinal axis of the pipe nˆ f , and η is the coordinate along the pipe (unit vector nˆ p , see Fig. 6.1). Assuming that. 1. the main contribution of the flux in the right-hand side integral of (6.13) comes from the adjacent fractures, thus neglecting the part of the integral involving the contact between the lateral surface of the pipe and the porous matrix, and that 2. the hydraulic head in a given cross section is constant (it depends only on η, the local coordinate along the pipe), then (6.13) can be expressed in the following way − Ap k p

∂2 hp = ∂η2

mf

∑w

f , iv f , n,i ,

(6.15)

i =1

where i labels each adjacent fracture element to the pipe. 6.2.1.5 Flow in pipe connectors In the same way that fractures intersect each other creating channels, an arbitrary number of channels might intersect each other creating pipe connectors. These objects can be regarded as closed volumes of similar extension in all directions and comparable with the mean diameter of all the convergent channels Ap . By analogy, it is consistent to represent channel connectors by points called multiple pipe connectors (MPCs), disregarding their 3D structure by integration in volume. Thus, in an MPC, the following 0D version of the mass conservation is considered for the flow: mp

∑A

pi

⋅ vη ,i = 0,

(6.16)

i =1

together with the continuity of hydraulic heads h p ,1 = h p ,2 = ... = h p , m p ,

(6.17)

where mp is the number of pipes converging to the point. 6.2.2 Transport This section presents the governing equations in the porous matrix, a single fracture, a single pipe, and a single MPC. It is considered that all these entities offer

166 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES the same kind of discontinuity for both flow and transport problems, so the derivation in this case is similar to the one for the flow, being the only difference the leading operator of the partial differential equation (PDE). Finally, the formulation for the complete problem where all the entities interact at the same time is the result of solving all the equations together. The description of the coupling strategies will be treated in the next two sections. 6.2.2.1 General formulation In general, the transport process under consideration can be described by the advection–diffusion reaction equation for the concentration of pollutant: R

∂c + ∇ ⋅ q = K r c + ρ, ∂t qi = vi c − Dij

∂c , ∂x j

Dij = D M + αLPij (v) + αT ( δij − Pij (v) ) v,

(6.18) (6.19) (6.20)

where R is retardation factor, q is solute flux, Kr is reaction constant, ρ is a source, Dij is the dispersion coefficient; DM is the molecular diffusivity; αL and αT are the longitudinal and transversal dispersion coefficients, respectively, and P(v) is the projection operator onto the direction of the velocity vector v.

v = v (lx xˆ + l y yˆ + lz zˆ ) lx lx  P (v ) =  l y l x  l z l x

lx l y lyly lz l y

lx lz   l y lz  . l z l z 

(6.21)

(6.22)

In order to simplify the notation in the following sections, it is practical to define the p-dimensional advection–diffusion reaction operator Lχp applied on the entity χ by: Lψ p := Rψ

∂u ∂ ∂2 + vψ ,i − Dψ − kr , ∂t ∂ xi ∂ xi 2

(6.23)

where the subindex χ can be any of m, n or p identifying the porous matrix, a single fracture, or a pipe element , respectively; the index p is the dimensionality (1, 2 or 3); and i = 1,…, p. Then, the general formulation for the transport in any entity of the FPM can be summarized in the following expression:

Lpχ [cχ ] = ρχ ,

(6.24)


167

Table 6.1: Entities involved in the problem and their possible dimensionality. Dimension p Entity

χ

3D case

2D case

Porous matrix Fracture Pipe MPC

m f p o

3 2 1 0

2 1 0 –

where ρχ changes according to χ and p, and represents the coupling term between entities. Table 6.1 summarizes the possibilities. 6.2.2.2 Transport in the porous matrix Both, the small variation of concentration and the assumption of low compressibility of the fluid allow us to neglect any change of the density, and to keep the approximation of the irrotational steady state velocity field. In addition, considering a homogeneous isotropic media, the concentration in the porous matrix is described by (6.24) with χ = m and ρm = 0 . (For simplicity, the theory is presented for homogeneous properties, in spite of the fact that the numerical method explained in the next two sections, has been developed for non-homogeneous piecewise constant diffusion coefficients.) 6.2.2.3 Transport in a single fracture Integration of (6.19) along z' in the same way as was done in the flow problem yields

ρf =

1 wf

∑q

m , n ,i ,

(6.25)

i = A ,B

where qm, n,i = q ⋅ nˆm,i is the normal concentration flux coming from the porous matrix. Thus, the influence of the two blocks of porous matrix (A and B) adjacent to the fracture is considered as a source term for the fracture. Finally, the formulation for a single fracture is represented by (6.24) and (6.25) with υ = f . 6.2.2.4 Transport in pipes Integration of (6.18) over the cross section of a channel yields the 1D formulation for pipes, represented by (6.24) with χ = p and the source term given by:

ρ p (η, t ) =

1 Ap

∫v

f ,n c f

(η, s, t ) − D f ∇ 2D c f (η, s, t ) ⋅ nˆ dΓ

Γ

being η the coordinate along the pipe.

(6.26)

168 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES 6.2.2.5 Transport in pipe connectors Similarly to the flow problem, the 3D structure of an MPC is collapsed into a point where L0o is identically zero, and the source term of (6.24) becomes:

∫q

ρo (η, t ) =

p, x

⋅ nˆdSo .

(6.27)

∂Vo

Thus leading to the continuity of concentration c p ,1 = c p ,2 = ... = c p , mp

(6.28)

and the conservation of the normal flux of concentration mp

∑A q p

p , n,i

= 0.

(6.29)

i =1

6.3 Numerical method 6.3.1 Introduction This section presents a general overview of the numerical scheme to be implemented. In Section 6.3.2 the main steps of the BEM are summarized, a complete introduction to the method can be found in Brebbia et al. [25]. Section 6.3.3 describes the dual reciprocity method (DRM) which is used to solve the domain integrals that appear in the integral formulation of the governing equations. Finally, the third part describes the time integration scheme and the domain decomposition technique. 6.3.2 The boundary element method 6.3.2.1 Integral formulation The numerical implementation of the BEM requires the discretization of the boundary into elements, and this represents one of the most powerful advantages of the method, since there is no need to discretize in volume. The starting point of the BEM is the integral formulation of the governing differential equation. The governing equation that describes a linear time-dependent process of flow and transport in porous media, in a general form in a domain Ω, can be written as

∇ 2 u = b ( x, y , u , t ) ,

(6.30)

where the boundary conditions are defined as u=u

on Γ1

(6.31)


169

and q = ∂u ∂n = q

on Γ2.

(6.32)

Here Γ = Γ1 + Γ2 is the exterior boundary that encloses the domain Ω and n is its outward normal. For the flow equation, u represents the hydraulic head h and therefore according to (6.1) the non-homogeneous term b has the following form: b=

1 ∂h   −Qe + Sr  , ∂t k

(6.33)

while for the transport, u ≡ c(xi, t) and according to (6.18) and (6.19) for scalar dispersion coefficient the non-homogeneous term b has the following form: 1  ∂c   R + ∇ ( νi c ) − K r c − ρ , D  ∂t

b=

(6.34)

where vi = − k (∂h / ∂ xi ) represents the ith component of the velocity vector v shown in (6.6). Applying the Green integral representation formula to (6.30), it is found that the value u at a point x within the domain Ω, is given by [25]:

∫

∫

λ ( x)u ( x) + q* ( x, y )u ( y )dΓ y − u* ( x, y ) q( y )dΓ y Γ

Γ

∫

(6.35)

= u* ( x, y )b( y )dΩ y Ω

Here, u*(x, y) is the fundamental solution of the Laplace equation, which for an isotropic 2D medium is given as: u * ( x, y ) =

1 1 log , 2π r

(6.36)

1 1 , 4π r

(6.37)

and for a 3D case becomes: u * ( x, y ) =

where r is the distance from the point of application of the concentrated unit source to any other point under consideration, i.e. r = |x – y|, q(y) = ∂u(y)/∂n and q*(x, y) = ∂u*(x, y)/∂n and n is the normal to the boundary. Note that in (6.35) all the integrals are over the boundary Γ of the domain, therefore these are surface integrals, except for the one corresponding to the term b(y), which is performed

170 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES over the domain Ω, and therefore this is a volume integral. The term b(y) represents the sum of the non-homogeneous terms, see (6.33) and (6.34), and is defined according to the model and process under consideration. The constant λ(x) has values between 0 and 1, where for a smooth boundary it is equal to 1/2, and for points inside the domain λ(x) is equal 1. More information on how to calculate λ(x) can be found in Brebbia et al. [25]. Equation (6.35) represents the integral formulation of (6.30), and is the starting point of the applied BEM formulation. 6.3.2.2 Boundary discretization The three terms on the left-hand side of (6.35) involve only boundary integrals. The boundary Γ can be discretized into Ne3D elements. In the 3D case, the integration domain Ω (used to represent the porous matrix blocks) is a volume, and its boundary Γ is discretized by means of a collection of connected triangular or quadrilateral isoparametric elements. In the 2D case, the boundary is represented by lines and the integration domain Ω is a surface. The path enclosing Ω is the boundary, which is discretized into Ne2D linear elements. The BEM for the 1D case will be used to represent pipes when intersections between fractures in the fracture network occur. The integration domain (Ω) is a linear straight segment and their two geometrical endpoints become the boundary (Γ), and each one of them represents a boundary element. In general, Γ is discretized into Ne boundary elements, according to: Γ = Γ1 ∪ Γ 2 ∪ ... ∪ Γ Ne , so that Ne

ci ui +

∑∫

j =1 Γ j

∂u* ud Γ − ∂n

Ne

∑∫u j =1 Γ j

*

∂u dΓ + bu *dΩ = 0. ∂n

∫

(6.38)

⑁

The treatment of the domain integral that appears in the last term of (6.38) will be deferred for the next section. Each boundary element contains a number Nfn of subjacent collocation nodes, where the potential or fluxes are evaluated. In this way, the values of the potential or its normal derivative at any point defined by the local coordinates on a given boundary element can be defined in terms of their values at the collocation nodes, and the Nfn interpolation functions in the following way: u (ξ ) =

N fn

∑ ψ (ξ ) u k

(6.39)

k

k =1

and

∂u ( χ) = ∂n

N fn

∂u

∑ υ ( χ) ∂n k

k =1

. k

(6.40)


171

With the discretization of the boundary and using the collocation technique, expression (6.38) can be rewritten in the following way: Ne

ci ui +

∑∑ ∫ j =1

Ne

−

  *  ∂u θk dΓ j  ukj  ∂n j  k =1  Γ j  N fn

   u *θk dΓ j  ∂u + bu *dΩ = 0.   ∂n kj k =1  Γ j  ⑁ N fn

∑∑ ∫ j =1

∫

(6.41)

The notation can be simplified by making use of matrix notation, so the last expression can be written in the following way:  ∂u  Hu − G   = − bu*dΩ ,  ∂n 

(6.42)

∂ui* ∂n j

(6.43)

∫ ⑁

where H il = δil ci +

∫

Γj

υk ( χ j )dΓ j , χj

and Gil =

∫ u (ξ )ψ (ξ )dΓ , * j

j

k

j

j

(6.44)

Γj

where the index l = 1, … ,Nfe and Nfe = ∑ Nj =e 1 N fn, j is the total number of collocation nodes adjacent to a given domain. In fact, the index l is used to identify one of the adjacent freedom (collocation) nodes from a global point of view, and is given as a function of the indicator of element (j), and the local collocation node of that element (k). The boundary element dΓj can be expressed in terms of the domain local coordinates (ξ) through the Jacobian of the transformation J in the following way:

dΓ j = J dξ1 L dξ h ,

(6.45)

where h is the dimension of Γ. Finally, provided that the right-hand side term of eqn (6.42) can be written as a given vector in function of the source term, or a characteristic matrix in function of the unknown potentials and normal fluxes at the collocation nodes of the boundary, the application of the prescribed boundary conditions and the assembly of the linear set of equations, that (6.42) produces, yields to a determined system of equations of dimension Nfe × Nfe of the form Ax = b,

(6.46)

172 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES where the vector of unknowns (x) contains the potentials and normal fluxes that were not prescribed as boundary conditions. The matrix A contains the coefficients of H and G, and the right-hand side term contains the non-homogeneous term and the boundary conditions. 6.3.2.3 Internal solution Once the problem given by (6.46) is solved, it is possible to calculate the values of the fluxes ∇u ( xi ) and potentials u(xi) at any internal (observation) node xi by means of the integral eqn (6.41). Therefore, the potential at xi becomes: N fe

ui =

∑ j =1

 ∂u j   ∂ n  Gij −  

N fe

∑u H j

(6.47)

ij

j =1

and the gradient of the potential can be obtained with:

∂u ∂ xp

N fe

= xi

∑∫ j =1 Γ j

∂ u j ∂u* dΓ j − ∂n ∂ xp

N fe

∑∫u j =1 Γ j

j

∂ ∂ xp

 ∂u*   ∂ xp

  dΓ j . 

(6.48)

6.3.3 The dual reciprocity method This section gives an overview of DRM including the radial basis function considered, and the strategy for the reactive, advective, and time-dependent term. The previous section gave a general overview of the BEM for the Poisson equation, avoiding the treatment of domain integrals. In general, domain integrals arise from linear but non-homogeneous terms, non-linear terms, or time-dependent terms. In this case, the non-linear term in (6.42) introduces one of those domain integrals in (6.36). The most familiar techniques used to solve domain integrals are, direct numerical approximation, elimination of non-homogeneous terms via exact or approximate particular solutions, and dual and multiple reciprocity methods. In principle, the domain integral would require some internal discretization in which case the complete scheme would loose one of its main attractions, which is being based on a ‘boundary-only’ discretization. Although internal discretization has been extensively used in the past, e.g. in the cell integration method [26], providing accurate results for a variety of PDEs, it has the main disadvantage of requiring an extra amount of data such as internal connectivities, hence making the code more complex and more demanding in terms of computational resources. Here, the DRM is proposed in order to avoid this inconvenience. The DRM was introduced by Nardini and Brebbia [27] and subsequently used in various applications. A thorough introduction to the method can be found in Partridge et al. [28].


173

The main idea is to transform the domain integral that appears in (6.42) into an integral over the boundary by means of a finite set of interpolating functions, as explained in the next section. 6.3.3.1 General approach The non-homogeneous term b in (6.30) can be written as a linear combination of the approximating functions fj Nr

∑ α f (x),

b( x) =

j

(6.49)

j

j =1

where Nr is the number of functions required for the approximation and αj are undetermined coefficients. The approximating functions are linked to the particular solution uˆ of the Laplace operator through ∇2 uˆ j = f j .

(6.50)

Thus, eqn (6.30) can be written in the following way: Nr

∑ α ∇ uˆ .

∇2 uˆ =

2

j

(6.51)

j

j =1

In the last expression it is possible to apply the weighting procedure with the fundamental solution in order to produce the integral equation

∫(

∇2u

)

Nr

u*dΩ

=

∑ α ∫ (∇ uˆ ) u dΩ. j =1

Ω

2

j

j

*

(6.52)

Ω

Applying the Green integral representation formula and the subsequent discretization of the boundary, as it was described in the previous section, yields the following integral equation, for the source point located at the ith collocation node: N fn

∑H

N fn

ik uk

k =1

−

∑G

ik

k =1

 αj  =  j =1  Nr

N fn

∑ ∑ k =1

∂ uk ∂n

  H ik uˆkj  −     

∂ ukj  , Gik ∂n  k =1  N fn

∑

(6.53)

174 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES where uˆij = uˆ j (xi )

(6.54)

is the jth particular solution evaluated at the ith collocation point, and

∂uˆkj ∂uˆ j (x k ) = ∂n ∂ n[ k ]

(6.55)

is the derivative of the jth particular solution evaluated at kth collocation node in the direction of the outward normal of the boundary element that contains the kth node. The vector of coefficients (αj) in eqn (6.53) can be obtained by solving the linear system: F ␣ = b,

(6.56)

where b = b(xi) is the vector containing the non-homogeneous terms evaluated at the collocation nodes. Finally, it is more practical to rewrite eqn (6.53) in the following matrix notation: Hu − G

∂u = Sb, ∂n

(6.57)

where the following DRM matrices have been defined ˆ = uˆij U ˆ = ∂ uˆ j (x k ) Q ∂ nk ˆ F −1 . ˆ − GQ S = HU

(

)

(6.58)

6.3.3.2 Radial basis functions In principle, any set of approximation functions f could be used in the DRM formulation. The only restriction is that the resulting matrix F must be non-singular. At the same time it is desirable to minimize high amplitude oscillations without excessively smoothing the interpolation. The interpolating functions used in this work for the transport problem in the fractures, and in the porous matrix were the so-called augmented thin plate splines [29], whereas the solution in the pipes, is based on cubic splines and Lagrange polynomials. Table 6.2 summarizes the sets of interpolating functions used in each case. When an element of matrix F is represented by a radial basis function (RBF), then the following notation is equivalent: f ij = f j ( xi ) = f (rij ) , where

rij is the distance between the collocation nodes i and j.

(6.59)


175

Table 6.2: Sets of interpolating functions used. Entity Porous matrix Fracture Pipe MPC

Dimension

Set of interpolating functions

3D 2D 1D 0D

{r, 1, x, y, xy} {r2log(r), 1, x, y} Cubic splines –

6.3.3.3 The reaction term The reaction term (−kr u(x)) involves the evaluation of the unknown field u in the domain. Applying the same set of interpolation functions as in (6.49) to u, i.e. u = ∑βj fj, where the set β is different from the set α used in (6.49), and inverting F it is straightforward to express the potential at any point inside the domain in terms of its values at the collocation nodes. In this way, the reaction term contributes with the vector bREACT ,i = − kr ui ,

i = 1, ... , Nfn

(6.60)

6.3.3.4 The convective term The convective term introduces a first order derivative in space and is represented by:

∇ ( vu ) = v ⋅ ∇u + u ( ∇ ⋅ v ) .

(6.61)

The value of ∇u at any point inside the domain can be expressed in terms of F by means of:

∂ u ( x) = ∂ xp

Nr

∑α

j

j =1

∂ f j ( x) . ∂ xp

(6.62)

And the coefficients αj can be obtained by inversion of F as shown in (6.56). In the case of incompressible flow the second term in (6.61) vanishes, while the first one contributes to the discrete non-homogeneous term b in (6.57) according to: bCONV ,i =

∑V

ikp Tkjp u j ,

(6.63)

k , p, j

where Vikp = δik vkp Tkjp =

∂ f kl −1 flj , ∂ xp

(6.64)

176 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES where the subindex p stands for the components of Cartesian coordinates (x, y, z) in the 3D case or (x', y') in 2D, while subindices i, j, k, l represent the collocation nodes in the domain. 6.3.3.5 Time integration scheme The integration in time is based on the Finite Difference time marching scheme. A two time-level scheme has been implemented such that the time derivative is approximated in the following way:

∂ c c m +1 − c m ≈ ∂t δt

(6.65)

and the concentration c and its flux q are given by: c ≈ θc c m +1 + (1 − θc ) c m

q ≈ θq q m +1 + (1 − θq ) q m .

(6.66)

Superscripts m and m+1 indicate previous and present time levels, respectively. The coefficient θi can be adjusted from 0 to 1 yielding different schemes (Crank Nicholson, Euler implicit, Euler explicit, or any intermediate scheme). The time step δt is recalculated at every time level such that the maximum variation of concentration ∆c /c remains bounded below a certain arbitrary threshold ≈0.05, according to:  c  δt m < κ    ∂ c ∂t 

m −1

.

(6.67)

This is done in order to increase the time step when the solution is closer to its steady state, thus reducing the number of time steps and CPU requirements. This represents an important advantage when using iterative solvers, for the final system of equations. For small problems with less than 2000 degrees of freedom, a direct solver is preferred instead of an iterative one, since the factorization of the system is calculated only once at the beginning for the initial time level, and then, further time levels involve only recalculation of the right-hand side term and matrix back-substitution operation, which are, by far, less demanding from a computational point of view than the matrix factorization. However this can be done only if the time step ∆t remains fixed at every time step. As a conclusion, for small problems it is more efficient to keep ∆t fixed and use a direct solver, whereas for large problems it is better to allow time step adaptivity according to expression (6.67) combined with an iterative solver. 6.3.3.6 Domain decomposition and DRM–MD The DRM has been demonstrated to be a general and reliable procedure. However, soon it became clear that there are some problems associated with this


177

numerical technique. The first one was related to the fact that a number of interior DRM nodes were required in order for the interpolation, see (6.49), to be more accurate. The problem associated with this was that no procedure was available for defining the optimal position of the nodes in the interior of the domain, though it was observed that this distribution significantly affects the accuracy and stability of the solution. Also, as many of the RBFs used are globally supported the matrix of the resulting system of equations is dense and frequently ill conditioned, when applied to large problems. This makes the method computationally expensive and sometimes unstable when applied to large problems. There are two ways to avoid these difficulties: by using compactly supported RBFs (CS-RBFs) or by using domain decomposition. Domain decomposition is a technique that is commonly used in the BEM when the domain is piecewise homogeneous. After applying the numerical formulation in every subdomain, the final system of equations is obtained by means of a set of matching conditions in the interfaces between subdomains. The resulting system of equations is not dense, and the sparsity of the system increases with the number of subdomains. A combination of domain subdivision and the DRM to avoid the domain integral was implemented by Popov and Power who called the scheme the dual reciprocity method−multi-domain (DRM–MD) approach. The initial problem solved using this formulation was the flow of a mixture of gases through a porous media [30–32]. The DRM–MD has also been applied to linear and nonlinear advection-diffusion problems [33], driven cavity flow of Navier-Stokes equations [34] and of non-Newtonian fluids [35], and the flow of polymers inside mixers with complex geometries [36]. More recently the DRM–MD has been applied to a comparison of the equivalent continuum, non-homogeneous and dual porosity models for flow and transport in fractured porous media [37], 3D convection-diffusion problems [38] and flow and solute transport in 3D fractured porous media [39]. Matching conditions between two adjacent subdomains A and B must be satisfied as shown in (6.68) u A = uB

[q ⋅ nˆ ] A = − [q ⋅ nˆ ]B ,

(6.68)

where u denotes the potential (concentration for the transport problem, or hydraulic head for the flow problem), q is the flux of that quantity, and nˆ is the outward normal unitary vector to the boundary of the subdomain. In this way, the formulation can deal with piecewise homogeneous material properties. Moreover, by increasing the mesh refinement it is possible to solve problems with strong variations of the material properties or the solution fields, in spite of dealing with meshes more similar to the ones employed by the finite elements method or finite volume methods. The DRM–MD does not suffer the two main problems related to standard DRM; the systems of equations produced by DRM–MD are sparse and well

178 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES conditioned, and the number and position of DRM nodes is usually not critical, since small subdomains usually require none or very few interior DRM nodes, which can be placed on equal distance in the interior of the domain. The matrices derived from the domain decomposition techniques are sparse; the higher the domain discretization the larger the number of zero entries in the matrix. This becomes a desirable advantage, since sparse matrices can be efficiently solved with many iterative techniques like Krylov based solver, conjugate gradients, etc. On the other hand the increase of discretization implies an increase in the number of degrees of freedom, this is the price to pay in order to obtain reasonable sparsity patterns. Therefore it is predictable that neither the extreme multidomain (MD) decomposition nor the classical single domain (SD) approach would offer the optimum solution in terms of computational efficiency for an arbitrary problem, but an intermediate between both. This suggests the idea of a flexible hybrid method in which some regions of the domain can be treated with MD and some others with SD discretization. Such application of the DRM–MD technique has been suggested by Popov and Power [30, 33], but was implemented for the first time by Samardzioska and Popov [37] in 2D and by Peratta and Popov [39] in 3D. Some analysis addressing the accuracy, efficiency and stability of this approach as a function of the different discretization options is shown in [40].

6.4 Computational implementation Bellow the main features of the developed computer code are summarized: • The solver is based on the discrete fracture network model. • The model for flow is based on the Darcy flow and for the transport on the advection-dispersion equation with reaction. • The rock (3D entities), the fractures (2D entities), the fracture intersections (pipes – 1D entities) and pipe intersections (0D entities), have been implemented and coupled in a 3D code. • The numerical approach used is the BEM with domain decomposition for the flow and boundary element–dual reciprocity method–multidomain (BE– DRM–MD) approach for the transport; as explained in the previous section. • The computer code is implemented in such way that many subdomains with different geometries and properties can coexist in a singe model. • The way in which the scheme is implemented offers unique flexibility to decide whether certain subdomain, 3D or 2D, would be taken as a single domain, or would be decomposed in subdomains. • Manual or automatic fracture intersection detection. • Automatic time step selection. • The code is linked to the commercial package GiD for pre- and postprocessing. • The main problems encountered during the development of the method/solver were related to the different time scales of the processes in different media.


179

Coupling Strategy

POROUS MATRIX

PI PE

POROUS MATRIX

POROUS MATRIX

FRACTURE

POROUS MATRIX

3D BLOCK Porous matrix 2D SURFACE Fracture 1D PIPE Fracture Intersection 0D MPC Pipe Intersections

Figure 6.2: Coupling of porous matrix blocks, fractures and fracture intersections. For example, the processes in rock and clay were of at least two orders of magnitude slower than in the fracture zones and excavation-disturbed zone (EDZ). These problems were successfully resolved by applying a semianalytical approach. • The code shows high accuracy and capability to integrate geometry with small details inside large-scale models. Figure 6.2 shows the way that matrix blocks, fractures and fracture intersections interact. Fractures can be modelled as 2D or 3D entities. The following solvers and pre-conditioners for sparse system of equations were implemented: • direct solvers – LU (Gauss + Pivoting + dropping technique to keep the sparsity pattern) • iterative solvers (sparskit) [41] – GMRES–FGMRES–PGMRES – CG – FOM – BICG • preconditioners – ILUT, ILTP, ILUT(n) – Sparskit [41] – MC64 – physical and geometrical scaling. Figure 6.3 shows different possibilities available for representing 3D porous volumes. The 3D subdomains can either be discretized by volume using linear or


Shape Functions

Quadratic Elements

Automatic Sub-domains Volume meshing using tetrahedrons or hexahedrons

Manual sub-domains (Geometry modeller & Surface meshing)

Optional internal nodes for the DRM

Linear Elements

Figure 6.3: Various possibilities for discretization of porous blocks. quadratic tetrahedrons or hexahedrons, or can be discretized over the surface of the volume.

6.5 Results This section contains the findings on the safety assessment of the proposed LowRiskDT approach for disposal of hazardous waste in abandoned underground mines. The safety criterion related to the waste isolating capacity of the mine repositories is evaluated taking into account the quality of the groundwater on a certain distance from the mine in the direction of the flow of the groundwater. Since no particular mine has been considered, an imaginary scenario is created where two different types of host rock media are considered: crystalline rock and limestone. All the considered parameters of the models were chosen in a conservative way or worst-case scenario, so should the findings be in favour of the approach, a sufficiently large safety margin would exist. Both cases of mine repositories in crystalline rock and limestone were of similar geometry. The mine in crystalline rock consists of a room and a tunnel. Around the room and the tunnel EDZ was considered in the model. Eighteen fracture zones intersect the domain, of which three intersect the EDZ and serve as fast tracks for transport of contaminants. The mine in limestone consists of a room and no EDZ was considered around the repository. No fracture zones were considered for the case of mine repository in limestone. The analysis for both mine repositories was done for two types of chemicals: dichlorvos and batteries/zinc.


181

Two types of analysis were performed, long-term, for periods of up to 600,000 years, and short-term, for periods of up to few thousand years. 6.5.1 Types of geological media considered The evaluation of waste-isolating capacity in mine repositories regarding the flow and transport aspects is conducted for two different geological media, crystalline rock and limestone. In the case of crystalline rock the model consists of a large room, a tunnel, an EDZ of variable thickness around the room and the tunnel, intersecting fracture zones, and chemicals, which are embedded in compacted clay inside the room and the tunnel. In the case of limestone the model consists of a large room and chemicals, which are embedded in compacted clay inside the room. 6.5.2 The waste types considered The waste types considered are dichlorvos and zinc (Zn). 6.5.2.1 Dichlorvos Dichlorvos is an organophosphate insecticide with the chemical name 2,2dichlorovinyl dimethyl phosphate. Common trade names are Astrobot, Atgard, Canogard, DDVP, and Vapona. Some of the properties of dichlorvos are as follows [42]: • • • • • • •

colourless liquid with a mild chemical odour, aromatic odour; molecular weight: 220.98; boiling point: 117°C at 10 mm Hg; solubility: 10,000 ppm at 25°C; vapour pressure: 1.2 × 10–2 mmHg at 20°C; octanol–water partition coefficient: log Kow = 1.4; chemical formula: (CH3O)2(P=O)OCH=CCl2;

The information on the environmental fate of dichlorvos originates from studies designed to assess its use as an insecticide. Aerobic soil metabolism data showed a half-life of 0.42 days in a sandy loam soil at pH 6.2. The major metabolites were 2,2-dichloroacetic acid (DCA) (62.8% of applied dichlorvos at 48 h). Anaerobic soil metabolism in a sandy loam soil (water flooding and nitrogen atmosphere) at pH 6.8 at 25°C resulted in a half-life of 6.3 days. The major non-volatile products were DCA (accounting for up to 50.9% of applied radioactivity at day 60), 2,2dichloroacetaldehyde (accounting for up to 12.6% of applied radioactivity at day 5), and 2,2-dichloroethanol (accounting for up to 24.7% of applied radioactivity at day 60). The potential to leach to groundwater after its application to soil is rather low, due to its rapid degradation. As the half-life of dichlorvos is very short compared to the time-scale considered for the safety assessment, it was decided to effectively follow the transport

182 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES of DCA, the main decomposition component of dichlorvos, and also the most toxic by-product. For this chemical, maximum allowable concentrations in drinking water have been imposed. For example, the US EPA has imposed a maximum contaminant level of 60 µg/L in drinking water for the average annual concentration of the sum of monochloro-, dichloro- trichloro-, monobromo-, and dibromoacetic acids [43]. The World Health Organization has a recommended level of 50 µg/L for DCA in drinking water [44] and Australia and New Zealand recommended a level of 100 µg/L [45]. The reported literature data do not mention the amount of DCA expected from dichlorvos decomposition. However, the maximum expected concentration (conservative case) of DCA would correspond to a molar ratio of DCA : dichlorvos = 1 : 1 or respective weight ratio of DCA : dichlorvos = 129 : 221 = 0.58. Thus, the maximum expected DCA concentration in mg/L would be: (maximum dichlorvos concentration, mg/L)(0.58). Due to its high solubility in water and the presence of 2-propanol, a reasonable and also conservative sorption coefficient for DCA in all cases would be Kd ≅ 0. The decomposition rate or the half-life for DCA is unknown and therefore following the conservative approach regarding the safety assessment, no decomposition of DCA will be considered. 6.5.2.2 Zinc Zinc was selected as second chemical that would be considered when the waste isolating capacity in mine repositories is evaluated. Zinc would appear in the repository as a result of batteries, which would be embedded in clay in the mine repository. Zinc occurs in the +2 valence state and forms many complexes and solid phases. At pH >13 expected in the alkaline battery waste, the predominant forms of zinc are [Zn(OH)3] − and [Zn(OH)4]2−, in equilibrium with Zn(OH)2(s). If significant concentrations of chloride anions (halite rock, sea water) or carbonate anions (carbonate rocks) are present, additional soluble species, such as ZnCO3(aq) and ZnCl+ may be formed. In Leclanche cells, the solid phases Zn(NH3)2Cl2(s) and ZnCl2.4Zn(OH)2(s) have been reported. 6.5.3 Case of mine and tunnel in crystalline rock The first case is a mine repository in crystalline rock, which includes a room and a tunnel, where both the room and the tunnel are filled with chemical waste embedded in clay. 6.5.3.1 Geometry definition Figures 6.4 and 6.5 show the side view and the top view of the considered domain, respectively, including the geometry of the mine and the tunnel. The dimension of the room is 100 m × 50 m × 50 m. The room is filled with hazardous waste embedded in compacted clay. The length of the tunnel is 150 m and the


O3

x

183

Ground level g

y

O2 O1

Figure 6.4: Side view of the considered domain showing the geometry of the mine and tunnel and the respective position of the observation well.

x

(0,0,0) z

L

O1

L

Figure 6.5: Top view of the considered domain showing the geometry of the mine and tunnel and the respective position of the observation well.

184 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 6.3: Definition of observation points. Point O1 O2 O3

Position

Absolute coordinates (x, y, z)

Geometrical midpoint of the room In the well, at the room level In the well, at ground level

225, −400, 300 535, −400, 300 535, 0, 300

cross section is 5 m × 5 m. Around the room and the tunnel there is an EDZ with variable thickness, which is not shown in the figures. The width of the EDZ is 3 m around the room and 1 m around the tunnel. The vertical and horizontal lines in the figures represent fracture zones with a width of 1 m. It can be seen that there are 18 fracture zones in the model. The fracture zones are perpendicular to each other, separating in this way large porous rock blocks, being each one of them surrounded by six fractures. In this case perpendicular flat fracture zones were selected for simplicity reasons, when defining the fracture network, though the model and the computer code can cope with any shape and distribution of the fracture network. For each porous block the average hydraulic properties are considered. In Fig. 6.4 it can be seen that one fracture perpendicular to x-axis and one fracture perpendicular to y-axis intersect the EDZ of the room, while two fractures perpendicular to x-axis intersect the tunnel. In Fig. 6.5 it can be seen that one fracture perpendicular to z-axis intersects the EDZ of the room. This is considered to be a conservative case since three fracture zones intersect the EDZ of the room and two intersect the EDZ of the tunnel, which speeds up the transport of the chemicals, which would leak out of the repository. Figures 6.4 and 6.5 and Table 6.3 show the position of the observation well and observation points. The observation well and observation points are used in order to simulate the appearance of the chemicals in a certain place in the domain. It has been selected that the well is inside the fracture that intersects the EDZ of the room, as the fastest transport would exist in this fracture. Also, for the same fracture that intersects the room, which is perpendicular to the z-axis and is shown in Fig. 6.5, concentration change in time is followed on the top of the domain, or, the surface of the rock massif. 6.5.3.2 Model discretization In Fig. 6.6 the discretization of the domain into rock blocks, fractures and fracture intersections is shown. The position of the room and the tunnel in the model is shown in Fig. 6.7. The full model is divided into two domains, near field, represented with green colour in Fig. 6.6, and far field. The rock blocks in the near field are discretized by volume and the rock blocks in the far field are discretized on the boundary only. This gives possibility to obtain more information about the processes in the near field, to take into account the processes in the far field and


185

Pipe network

Fracture network

Figure 6.6: Discretization of the domain into rock blocks, fracture zones and fracture intersections (pipes). still to keep the size of the system of equations within desired limits. Table 6.4 shows the number of different entities included in the model (3D porous blocks, fractures, fracture intersections). 6.5.3.3 Parameter estimation The hydraulic and transport properties of the rock, fracture zones, clay and EDZ are shown in Table 6.5. The hydraulic conductivities were chosen of order of magnitude that can be considered to be conservative. In other words, considering that the room is in crystalline rock, it is not expected that the actual hydraulic conductivities would be higher than the used ones. 6.5.3.4 Boundary and initial conditions The boundary conditions for flow are shown in Fig. 6.8. On the top surface atmospheric pressure and on the bottom surface impermeable boundary conditions are imposed. One of the vertical surfaces has got 5% overpressure in respect to the hydrostatic pressure, while the other three vertical surfaces are with hydrostatic pressure. The hydrostatic pressure is not shown in Fig. 6.8. Saturated flow is assumed.


Room and Tunnel

Figure 6.7: Position of the room and the tunnel in the model.

Table 6.4: Number of geometrical structures included in the model. Number of freedom nodes Number of geometrical nodes Number of DRM nodes Number of 3D blocks Number of 3D subdomains Number of 2D subdomains Number of 1D subdomains Number of pipe intersections

188352 7526 14212 340 40290 10636 1788 1468

The initial conditions for transport are given by defining the amount of chemical that is stored in the room and tunnel. In other words, the concentration of the chemical in the repository will decrease in time as it will leak from the repository in the surrounding strata. It is assumed that at time t = 0 there is no hazardous chemical present outside the repository.


187

Table 6.5: Hydraulic and transport properties of different entities, which form the geometry of the case study. Parameter

Clay buffer

Rock–porous matrix

Fracture zones

EDZ

K (m/s) D (m2/s) R kr (1/s) Width (m)

1 × 10−10 1 × 10−10 1 0 –

1 × 10−9 1 × 10−9 1 0 –

1 × 10−7 1 × 10−7 1 0 1

1 × 10−7 1 × 10−7 1 0 3

Figure 6.8: Flow conditions for the crystalline case.

6.5.3.5 Results for flow The results for the flow in the case of crystalline rock are shown in Fig. 6.9. Figure 6.10 shows a close-up view of the hydraulic head and velocity field near the room. The hydraulic head is represented as a density plot over the fracture network, whereas the velocity field is represented as a vector plot. Typical values of the velocity in the rock matrix are two orders of magnitude lower than in the fracture network, which is due to the difference in hydraulic conductivities in rock and fractures. The maximum gradient of hydraulic head over the whole domain is ∇h = 0.05. The influence of the EDZ can be seen in Fig. 6.10. The flow is directed towards the EDZ on the inflow part of the EDZ/room, in the


Figure 6.9: Density plot of hydraulic head and vector plot of Darcy velocity in the fracture network.

Figure 6.10: Detail of the velocity field and hydraulic head close to the near field.


189

figure bottom-left side of the room, and away from the EDZ/room on the outflow part, in the figure top-right side of the room. This is a consequence of the higher hydraulic conductivity of the EDZ in respect of the surrounding rock, making the EDZ take larger part of the flow in the vicinity of the room. The effect of the EDZ is more evident in Fig. 6.11, which shows only the velocity field. 6.5.4 Case of disposal of dichlorvos in mine repository in crystalline rock The first case considered is for the chemical dichlorvos disposed of in underground mine. In the following sections the safety aspects of a hypothetic abandoned underground mine in which dichlorvos is disposed of in clay will be considered. 6.5.4.1 Modelling conditions for dichlorvos The transport is calculated for the DCA, product of decomposition of dichlorvos. The distribution coefficient Kd is taken to be 0, therefore, the retardation factor R is 1. The worst-case scenario is considered, when there is no decay of DCA.

Figure 6.11: Vector plot of Darcy velocity in the fracture network.

Depth of 100% water saturation, cm

190 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES 120 100 80 60 40 20 0 0

2000 4000 Time, years

6000

Figure 6.12: Movement of the wetting front assuming only diffusion with D = 10−9 m2/s. The simulation is done by considering that there is certain amount of solidified dichlorvos embedded in clay in the repository at time t = 0. Only DCA is followed, as dichlorvos, because of the very short half-life, does not travel far and very soon after deposition, in maters of months, completely decays. Note that the conservative approach has been followed in respect to saturation of clay, as it was considered that the clay is saturated at t = 0. The LowRiskDT document D2.2 [46] shows that for the Friedland Ton clay with density at water saturation of 1900 kg/m3, practically important wetting of the volume of clay-embedded waste will not commence until 4000 years after application, providing that the waste mass in the big room in this case is surrounded by a 100 cm ‘liner’ of Friedland Ton with the assumed density, see Fig. 6.12. This result is obtained without taking into account the impact of pressure-induced wetting. The initial concentration of dichlorvos in the repository is assumed to be 10,000 ppm. As part of the conservative analysis it is assumed that dichlorvos completely transforms into DCA. Therefore, shortly after the start of the simulation, the concentration of DCA inside the repository is equal to 10,000 ppm. 6.5.4.2 Transport results for dichlorvos As a test of the accuracy of the simulation we use the plot of the concentration in the ‘pipe’/fracture intersection, shown in Fig. 6.13 as a parallel bright line above the tunnel. The concentration of DCA in Fig. 6.13 has been normalized, where 1 corresponds to 10,000 ppm. The concentration plot, Fig. 6.14, starts after the room and finishes after the second perpendicular fracture that intersects the tunnel. It is evident that there is a jump in the concentration related to the point where the second perpendicular fracture connects the pipe with the tunnel. Thought there were many tests of the 3D solver towards various 1D analytical


191

Figure 6.13: Close-view of transport of DCA after 1000 years in the vicinity of the repository.

Concentration [ppm]

1000

100 200 yr 2000 yr 6000 yr

10

1

0.1 250

300

350

400

450

500

X [m]

Figure 6.14: The effect of the tunnel in the crystalline case, where a vertical fracture is crossing the tunnel at x = 400 m and affecting the transport in the fracture intersection under observation.


Figure 6.15: Normalized concentration distribution of DCA in the considered domain after 127,000 years. solutions that verified the accuracy, this example confirms the accuracy of the model in real 3D conditions. Figures 6.15 and 6.16 show the character of the transport. Since the hazardous waste is embedded in clay of low hydraulic conductivity, the chemical is slowly released in time. This is a case of contaminant source which changes the magnitude in time as the concentration inside the repository drops down. It can be seen that by t = 100,000 years the maximum concentration in the rock is still close to the repository since the concentration gradient inside the repository is still high enough to induce significant flux of contaminant. At t = 300,000 years the outflux from the repository has decreased significantly, so the highest concentration in the rock is not adjacent to the repository any more, and is due to contaminant, which escaped the repository in the past. Both effects in the transport of the chemicals are evident, the advection and the dispersion. The timescale of the whole process of release of the chemical from the repository in this case is of the order of magnitude of 600,000 years, and it is referred to this time-scale as a long-term analysis. The short-term analysis is of the order of few thousand years. One example of short-term analysis is shown in Fig. 6.13, situation shown at t = 1000 years. Figure 6.17 shows the results for long-term analysis of DCA transport through a fracture that intersects the EDZ of the repository and appears at the ground level.


193

Figure 6.16: Normalized concentration distribution of DCA in the considered domain after 317,000 years.

Figure 6.17: Long-term analysis of DCA concentration variation on the ground level in the fracture closest to the LL line (see Fig. 6.5).

194 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES The fracture can be seen in Fig. 6.5 and is the closest one to the LL line. The analysis has captured the moment of highest concentration at the ground level, approximately t = 200,000 years. The value for the highest concentration is close to 10 ppm. However, these results are obtained for a very conservative case and in a real case it is highly unlikely that the concentrations would reach such level, because of the following: 1. Not all of the dichlorvos would transform/decay into DCA. 2. There would be decay of DCA and it may be that no DCA ever reach the surface. However, no data on decay of DCA is available. 3. Fully saturated flow was considered. 4. The flow velocity vector, see Fig. 6.11, has got a significant upward (towards the surface) component, which in reality may not be the case.

Concentration (ppm)

The other aspect that must be mentioned is that any analysis longer than few thousand years is unreliable since by that time tectonic as well as glacial processes may completely change the situation. Figure 6.18 shows concentration variation in time in the middle of the room, point O1, and in the observation well, point O2, see Fig. 6.4. It can be seen that by 300,000 years very little of the contaminant left inside the repository. The maximum concentration inside the well in point O2 is estimated at t ≈ 200,000 years. The maximum concentration in point O2 is approximately 3 ppm, which is lower than the maximum concentration found in the point O3 in the well at the surface, see concentration of DCA in Fig. 6.17 for x = 535 m. The highest concentration in O3 is above 7 ppm. This effect is due to the vertical component of velocity 12000

3.5

10000

3 2.5

8000

2 6000 1.5 4000

Room Well

1

2000

0.5

0 0

200

400 600 Time (x 1000 yr)

800

0 1000

Figure 6.18: DCA concentration variation in time in the middle of the room, point O1 in Fig. 6.4, shown on the left axis, and in the well, point O2 in Fig. 6.4, shown on the right axis.


Concentration profiles in the well

Time [yr]

0.8

200

Concentration [ppm]

0.7

600 800

0.6

1000 1200 1400

0.5 0.4 0.3

1600 1800 2000

0.2 0.1

2200 2400

0 -0.1 -600

195

-500

-400 Depth [m]

-300

-200

2600 2800

Figure 6.19: Short-term DCA concentration variation in time in the well. vector, see Figs 6.11 and 6.16. Figure 6.17 shows that the concentration distribution at the surface changes in time due to the advection dispersion processes. The dispersion process makes the peak wider in time, while the advection process moves the location of the peak in the direction of the groundwater flow. Figure 6.19 shows the short-term analysis of the concentration of DCA in the observation well. It is evident that the concentration in the point O2 is higher than the concentration in the well at the surface, in the first few thousand years. The DCA concentration in point O3 is not shown in Fig. 6.19 as at y = 0 m DCA is still not present after 3000 years. The concentration of DCA is higher in O2 than in O3 due to the smaller distance between the point O2 and the tunnel and the room and also because two fractures intersect at O2, one vertical and one horizontal. These two fractures also intersect the EDZ, see Figs 6.4 and 6.5, which increases the transport rate. DCA reaches O3 later than it reaches O2, however, the maximum concentration of DCA in O3 at later stages exceeds the one in O2 for the reasons explained above. It is worth noting that the situation in O2 would be different than what is shown in Fig. 6.19 due to several factors: 1. It was considered that the clay is saturated at t = 0 years. As mentioned above, in the case of the Friedland Ton clay with density at water saturation of 1900 kg/m3, practically important wetting of the volume of clayembedded waste will not commence until 4000 years after application, see Fig. 6.12, providing that the waste mass in the big room in this case is surrounded by a 100 cm ‘liner’ of Friedland Ton with the assumed density. Therefore, at time t = 3000 years the chemical would have not left the repository at all, or very little would have leaked. 2. Not all of the dichlorvos would transform/decay into DCA.

196 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES 0.4 Concentration [ppm]

0.35 0.3 0.25 0.2 0.15 0.1 0.05 0 0

500

1000

1500

2000

Time [yr]

Figure 6.20: DCA concentration variation in time in O2 during the first 2000 years. 3. There would be decay of DCA. 4. Fully saturated flow was considered, which would not be the case in general. Even under such conservative/unrealistic assumptions, the concentration of DCA in O2 would not exceed 1 ppm in 3000 years. The results in Fig. 6.19 show that after 600 years the concentration in O2 will not exceed 0.05 ppm, which is equivalent to 50 µg/L, and is within the recommended highest concentration allowable by the World Health Organization of 50 µg/L for DCA in drinking water [44]. Figure 6.20 shows the DCA concentration variation in O2 in the first 2000 years. 6.5.5 Case of disposal of zinc in mine repository in crystalline rock Second analysis for mine repository in crystalline rock was performed for the case of waste containing batteries. In the following sections the safety aspect of disposal of batteries in abandoned underground mines will be discussed. 6.5.5.1 Modelling conditions for zinc The geometry of the mine tunnel and considered domain and all the parameters in the model remained the same except the ones mentioned below. It was considered that the batteries are mixed with Friedland Ton clay in ratio 50 : 50 by volume. It was assumed that at t = 0 years the clay is fully saturated and the batteries are decayed in a way that the zinc can travel through the clay and into the surrounding rock. It was further assumed that 25% of the batteries mass is due to zinc. In the case of zinc it was taken that Kd is 0.02 m3/kg and using the following equation

ρ Kd m it is estimated that the retardation factor is approximately R = 121. R = 1+


197

2.5 Time [yr] 48400

Concentration [ppm]

2

72600 1.5

96800 121000

1 0.5 0 -0.5 -700

-600

-500

-400

-300

-200

-100

0

Depth [m]

Figure 6.21: Zinc concentration variation in time in the well. 6.5.5.2 Transport results for zinc The results for leakage and transport of zinc are shown in Fig. 6.21. It can be seen that in this case the ‘short-term’ should refer to the period of 100,000 years. This is due to the retardation of the zinc during the transport through the surrounding rock, an effect which did not exist in the case of DCA. The same velocity field as in the case of dichlorvos/DCA is obtained for zinc, shown in Figs 6.9–6.11. Similar propagation pattern to the one shown in Figs 6.15–6.20 for dichlorvos/DCA is obtained for zinc, with the difference of slower propagation rate. Results in Fig. 6.21 show that in the period of 120,000 years the concentration of zinc in the observation well will not exceed 2 ppm. However, these results are obtained for a very conservative case and in a real case it is very unlikely that the concentrations would reach such level, because of the following factors: 1. In the analysis it was assumed that the clay is saturated at t = 0 years. 2. Fully saturated flow is considered. 3. It is considered that the batteries have decayed at t = 0 in such way that zinc is free to travel through the clay and surrounding rock. 4. It is not considered that the rock would absorb and immobilize part of the zinc, which would reduce the amount of zinc available for transport. The influence of the retardation factor R in the equations is to slow down the transport, it does not immobilize the zinc. 6.5.6 Case of mine in limestone The second case is a mine repository in limestone, which includes a room filled with batteries embedded in clay.

198 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table 6.6: Hydraulic and transport properties of different entities, which form the geometry of the case study. Parameter K (m/s) D (m2/s) R

Clay buffer

Rock

1 × 10–10 1 × 10–10 1

1 × 10–6 1 × 10–6 1

6.5.6.1 Geometry definition The geometry of the mine and domain is the same one that is shown in Figs 6.4 and 6.5, with the difference that in this case the following was excluded from the model: fractures, tunnel and EDZ. The observation well remains in the same place, see Figs 6.4 and 6.5. 6.5.6.2 Parameter estimation The hydraulic and transport properties of the rock and clay are shown in Table 6.6. The hydraulic conductivities were chosen of order of magnitude that can be considered to be conservative. In other words, considering that the room is in limestone, it is not expected in reality that larger values for hydraulic conductivities would exist, than the ones used in the examples. 6.5.6.3 Boundary and initial conditions The boundary and the initial conditions are the same as in the case of crystalline rock given in Section 3.2.4. 6.5.6.4 Results for flow The results for flow are given in Figs 6.22–6.26. Since there are no fractures in this model, the hydraulic head and the velocity field are shown in an arbitrary plane, see Fig. 6.22. Figure 6.23 shows part of the mesh used in the model, as well as the plane used to show the results. Figures 6.24 and 6.25 show the side view and the top view of the velocity field with the hydraulic head. Figure 6.26 shows the velocity field and hydraulic head in vicinity of the repository. In the figure the characteristic velocities of the model are shown in some points. It can be seen that the velocities in the limestone are of the order of 1 m/year, while inside the repository the velocities are of the order of 0.1 mm/year. This shows that the difference in the velocities is of four orders of magnitude, which is in agreement with the difference in hydraulic conductivities in the clay and limestone. The transport in the clay is predominantly by diffusion, while in the limestone it is combined, advection and dispersion.


199

Figure 6.22: Hydraulic head and velocity field for the case of mine repository filled with clay in limestone.

In this case since the EDZ is not included in the model, one can observe different velocity field than the one for the case of repository in crystalline rock. While in crystalline rock the EDZ makes the streamlines converge towards the repository and diverge from the repository, because of the higher permeability, see Fig. 6.10, in the case of repository in limestone, the absence of the EDZ makes the streamlines diverge towards the repository and converge from the repository, see Figs 6.25 and 6.26. 6.5.7 Case of disposal of dichlorvos in mine repository in limestone In the following sections the safety aspects of a hypothetic abandoned underground mine in which dichlorvos is disposed of in clay will be considered. 6.5.7.1 Modelling conditions for dichlorvos The modelling conditions for dichlorvos were the same ones that were used in the case of mine repository in crystalline rock and are described in Section 6.5.4.1.


Figure 6.23: Hydraulic head, velocity field and part of the model mesh used for the case of mine repository in limestone. 6.5.7.2 Transport results for dichlorvos Figures 6.27 to 6.31 show the results for leakage of DCA from the repository and its transport through limestone. All the results are for short-term analysis, up to 2000 years. The process of leakage and transport is similar to the one in crystalline rock where the chemical is slowly released mainly by diffusion, because of the low hydraulic conductivity of the Friedland Ton clay, and after that it is relatively rapidly transported through the limestone due to both, advection and dispersion. In this sense the process looks like a quasi steady-state as the distribution of the DCA in the space looks similar in respect to the highest concentration in the domain, what changes are the concentrations which decrease due to the decrease of DCA inside the repository, which in turn reduces the outflux of DCA. There is difference in the processes of transport of DCA once it leaves the repository, depending on whether the mine is in crystalline rock or limestone. In crystalline rock the main transport is conducted through fractures and fracture zones, since there the hydraulic conductivity is much higher than in the rock. The crystalline rock slows down the transport by absorbing the chemical, which penetrates the rock mainly by diffusion. In the case of repository in crystalline rock the transport will be mainly defined by the characteristics and


201

Figure 6.24: Side view of the hydraulic head and velocity field for the case of mine repository in limestone.

Figure 6.25: Top view of the hydraulic head and velocity field for the case of mine repository in limestone.


0.876 m/yr

1.356 m/yr

1.48 m/yr

Figure 6.26: Side view of the hydraulic head and velocity field near the mine repository in limestone.

Figure 6.27: Normalized concentration distribution of DCA in limestone around mine repository after 200 years.


203







205

6 y = -400m y=0

Concentration [ppm]

5 4 3 2 1 0 0

1000

2000 Time [yr]

3000

4000

Figure 6.32: Concentration in function of time in the observation well for DCA in limestone (blue: x = 535 m; y = –400 m; z = 300 m) and at the surface (red: x = 527 m; y = 0 m; z = 300 m).

distribution of the fractures and fracture zones. In the case of the limestone the transport through the rock is rapid, compared to crystalline rock, due to much higher hydraulic conductivity. Figure 6.32 shows the results for short-term analysis of DCA concentrations in two points A and B, see Fig. 6.31. The points A and B are equivalent to the points O3 and O2 in Fig. 6.4 for the case of crystalline rock. It can be seen that unlike the case of mine in crystalline rock, here the maximum concentration is reached relatively quickly, after only few hundreds of years, and it decreases from then onward. The maximum concentration is just above 5 ppm reached in approximately 300 years, and drops below 1 ppm in both points after 4000 years. However, these results are obtained for a very conservative case and in a real case it is very unlikely that the concentrations would reach such level, because of the factors mentioned before, which are for convenience repeated here again: 1. 2. 3. 4.

Not all of the dichlorvos would transform/decay into DCA. There would be decay of DCA. Fully saturated flow was considered. It was considered that the clay is saturated at t = 0 years. As mentioned previously, practically important wetting of the volume of clay-embedded waste will not commence until 4000 years after application, see Fig. 6.12. This is for the case when the impact of pressure-induced wetting is not taken into

206 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES account and providing that the waste mass in the big room in this case is surrounded by a 100 cm ‘liner’ of Friedland Ton with the assumed density. Therefore, at time t = 3000 years the chemical would have not left the repository at all, or very little would have leaked. 6.5.8 Case of disposal of zinc in mine repository in limestone Second analysis for mine repository in limestone was performed for the case of waste containing batteries. In the following sections the safety aspect of disposal of batteries in abandoned underground mines will be discussed. 6.5.8.1 Modelling conditions for zinc The geometry of the mine and considered domain and all the parameters in the model remained the same as for DCA except the ones mentioned below. It was considered that the batteries are mixed with Friedland Ton clay in ratio 50 : 50 by volume. It was assumed that at t = 0 years the clay is fully saturated and the batteries are decayed in a way that the zinc can travel through the clay and into the surrounding rock. It was further assumed that 25% of the batteries by weight is zinc. In the case of zinc it was taken that Kd is 0.02 m3/kg, and the corresponding retardation factor becomes R = 121. 6.5.8.2 Transport results for zinc The same velocity field as in the case of dichlorvos/DCA is obtained for zinc, shown in Figs 6.22–6.26. Figure 6.33 shows the results for zinc concentrations in two points A and B, see Fig. 6.31. It can be seen that the concentrations

Concentration [ppm]

140 y=-400

120

y=0

100 80 60 40 20 0 0

10

20 30 Time [x 1000 yr]

40

50

Figure 6.33: Concentration of zinc as a function of time in the observation well (blue: x = 535 m; y = –400 m; z = 300 m) and at the surface (red: x = 527 m; y = 0 m; z = 300 m).


207

are higher than in the case of disposal of batteries in mine repository in crystalline rock. However, these results are obtained for a very conservative case and in a real case it is very unlikely that the concentrations would reach such level, because of the following factors: 1. In the analysis it was assumed that the clay is saturated at t = 0 years. 2. Fully saturated flow is considered. 3. It is considered that the batteries have decayed at t = 0 in such way that zinc is free to travel through the clay and surrounding rock. 4. It is not considered that the rock would absorb and immobilize part of the zinc, which would reduce the amount of zinc available for transport. The influence of the retardation factor R in the equations is to slow down the transport, it does not immobilize the zinc.

6.6 Risk assessment summary The long-term analysis showed that the hazardous waste embedded in clay of low hydraulic conductivity is slowly released in time. It can be seen that both effects in the transport of the chemicals are evident, the advection and the dispersion in the rock, while the transport in the clay is mainly due to diffusion. The timescale of the whole process of release of the chemical from the repository is the order of 600,000 years. This is what is referred to as long-term analysis in this chapter. The short-term analysis is of the order of few thousand years. The analysis of mine repository in crystalline rock shows that very low concentrations of chemicals would appear in the groundwater not far from the mine repository and on the surface. In the case of DCA the concentrations on the surface do not exceed 10 ppm before t ≈ 200,000 years. However, these results are obtained for a very conservative case and in reality it is very unlikely that the concentrations would reach such level, because of the following factors: (i) not all of the dichlorvos would transform/decay into DCA; (ii) there would be decay of DCA and it may be that no DCA ever reach the surface; (iii) fully saturated flow was considered; (iv) the flow velocity vector has got a significant upward (towards the surface) component, which in reality may not be the case. It must be mentioned that any analysis longer than few thousand years is unreliable since by that time tectonic as well as glacial processes may completely change the situation. The short-term analysis of DCA leakage and transport shows that the concentration of DCA in the observation well would not exceed 1 ppm in 3000 years. This result is valid for very conservative case, since in reality there would be several factors that would reduce the concentration in the observation well, e.g. it was considered that the clay is saturated at t = 0 years. In the case of the Friedland Ton clay with density at water saturation of 1900 kg/m3, practically important wetting

208 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES of the volume of clay-embedded waste will not commence until 4000 years after application. This is valid if don’t take into account the impact of pressure-induced wetting and providing that the waste mass in the repository is surrounded by a 100 cm ‘liner’ of Friedland Ton with the assumed density, which was not the case in this study. Therefore, at time t = 3000 years the chemical would have not left the repository at all, or very little would have leaked. The analysis for disposal of batteries in mine repository in crystalline rock show the effects due to the retardation of the zinc during the transport through the surrounding rock, effect which did not exist in the case of DCA. Similar propagation pattern to the one found for dichlorvos/DCA is obtained for zinc, with the difference of slower propagation rate. The results of analysis show that in the period of 120,000 years the concentration of zinc in the observation well will not exceed 2 ppm. However, these results are obtained for a very conservative case and in reality it is very unlikely that the concentrations would reach such level, because of the following factors: (i) in the analysis it was assumed that the clay is saturated at t = 0 years; (ii) fully saturated flow is considered; (iii) it is considered that the batteries have decayed at t = 0 in such way that zinc is free to travel through the clay and surrounding rock; (iv) it is not considered that the rock would absorb and immobilize part of the zinc, which would reduce the amount of zinc available for transport. The overall risk assessment of disposal of hazardous chemicals similar to dichlorvos or batteries in mine repositories in crystalline rock show that the risk in short-term, few thousand years, are minimal for the groundwater and surrounding environment, providing that a proper engineered barrier is implemented. The long-term analysis is in favour of the approach as well, however, because of the reasons mentioned above, any results giving predictions for more than 1000 years must be taken with caution. There are similarities and differences in the processes of transport of DCA once it leaves the repository, depending on whether the repository is in crystalline rock or limestone. Both processes are similar in the process of release of the chemicals from the repository, the main mechanism for transport being diffusion in clay. The differences are in respect to the transport in the surrounding geologic media. In crystalline rock the main transport is conducted through fractures and fracture zones, since there the hydraulic conductivity is much higher than in the rock. The crystalline rock slows down the transport by absorbing the chemical, which penetrates the rock mainly by diffusion. In the case of repository in crystalline rock the transport will be mainly be defined by the characteristics and distribution of the fractures and fracture zones. In the case of the limestone the transport through the rock is rapid, compared to crystalline rock, due to much higher hydraulic conductivity and is due to both, advection and dispersion. The results for short-term analysis of DCA concentrations show that the maximum concentration in the observation well is reached relatively quickly, after only few hundred years, and it decreases from then onward. The maximum concentration is just above 5 ppm reached in approximately 300 years, and drops below 1 ppm after 4000 years.


209

These results, just like the ones in the case of mine repository in crystalline rock, are obtained for a very conservative case and in reality it is very unlikely that the concentrations would reach such level, because of the factors mentioned above. For the case of disposal of batteries in mine repositories in limestone it can be seen that the concentrations are higher than in the case of disposal of batteries in mine repository in crystalline rock, with maximum concentrations reaching over 120 ppm in 40,000 years. However, these results are obtained for a very conservative case and in reality it is very unlikely that the concentrations would reach such level, because of the factors mentioned above. The above risk analysis shows that the disposal in mine repositories in limestone should also represent a safe option providing that the engineered barrier can provide sufficiently high insulation. The analysis shows that the engineered barrier in the case of mine repository in limestone is more important than in the case of crystalline rock because of the ways of transport of chemicals through these two different types of geological media, which has been described in this chapter.

References [1] Bear, J., Tsang, C.-F. & de Marsily, G. (eds.), Flow and Contaminant Transport in Fractured Rock, Academic Press, Inc.: San Diego, 1993. [2] Bear, J. & Berkowitz, B. Groundwater flow and pollution in fractured rock aquifers. Development of Hydraulic Engineering, Vol. 4, ed. P. Novak, Elsevier Applied Science: Oxford, 1987. [3] Adler, M.P. & Thovert, J.-F. (eds.), Theory and Applications of Transport in Porous Media. Fracture and Fracture Networks, Vol. 15, Kluwer Academic Publishers: Dordrecht, 1999. [4] Barenblatt, G.I., Zheltov, I.P. & Kochina, I.N., Basic concepts in the theory of homogeneous liquids in fissured rocks. Journal of Applied Mathematics and Statistics, 24, pp. 1286–1303, 1960 [in Russian]. [5] Gerke, H.H. & van Genuchten, M.T., A dual-porosity model for simulating the preferential movement of water and solutes in structured porous media. Water Resources Research, 29(2), pp. 305–319, 1993. [6] Warren, J.E. & Root, P.J., The behaviour of naturally fractured reservoirs. Society of Petroleum Engineers Journal, 3, pp. 245–255, 1963. [7] Odeh, A.S., Unsteady-state behaviour of naturally fractured reservoirs. Society of Petroleum Engineers Journal, pp. 60–64, March 1965. [8] Snow, D.T., Anisotropic Hydraulic conductivity of Fractured Media. Water Resources Research, 5(6), pp. 1273–1289, 1969. [9] Brown, S.R. & Scholz, C.H., Closure of random elastic surfaces in contact. Journal of Geophysical Research, 90, pp. 5531–5545, 1985. [10] Gentier, S., Morphologie et Comportement Hydromechanique d’une Fracture Naturell dans une Granite sous Contrainte Normale PhD Thesis, Universite d’Orleans, 1986.

210 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES [11] Brown, S.R., Fluid flow through rock joints; the effect of surface roughness. Journal of Geophysical Research, 92(B2), pp. 1337–1347, 1987. [12] Moreno, L., Tsang, C.F., Tsang, Y. & Neretnieks, I., Some anomalous features of flow and solute transport arising from fracture aperture variability. Water Resources Research, 26(10), pp. 2377–2391, 1988. [13] Moreno, L., Tsang, Y.W., Tsang, C.F., Hale, F.V. & Neretnieks, I., Flow and transport in a single fracture: A stochastic model and its relation with field observations. Water Resources Research, 24(12), pp. 2033–2048, 1988. [14] Barton, N., Bandis, S. & Bakhtar, K. Strength, deformation and conductivity coupling of rock joints. International Journal of Rock Mechanics and Mining Sciences, 22, pp. 121–140, 1985. [15] Mourzenko, V.V., Thovert, J.-F. & Adler, P.M., Permeability of a single fracture; validity of the Reynolds equation. Journal de Physique II, 5, pp. 465–482, 1995. [16] Dienes, J.K., Permeability, percolation and statistical crack mechanism. Issues in Rock Mechanics. Proc. 22nd Symp. on Rock Mechanics, Berkley, University of California, August 1987. [17] Long, J.C.S., Remer, J.S., Wilson, C.R. & Witherspoon, P.A., Porous media equivalents for networks of discontinuous fractures. Water Resources Research, 18, pp. 645–658, 1982. [18] Cacas, M.C., Ledoux, E., Marsily, G.D., Tillie, B., Barbeau, A., Durand, E., Feuga, B. & Peaudecerf, P., Modeling fracture flow with a stochastic discrete fracture network: Calibration and validation. 1. The flow model. Water Resources Research, 26, pp. 479–489, 1990. [19] Mercer, J.W. & Faust, C.R., Geothermal reservoir simulation. 3: Application of liquid-and-vapor-dominated hydrothermal modelling techniques to Wairakei, New Zealand. Water Resources Research, 15(3), pp. 653–671, 1979. [20] Charlaix, E., Guyon, E. & Roux, S., Permeability of a random array of fractures of widely varying apertures. Transport in Porous Media, 2, pp. 31–43, 1987. [21] Robinson, P.C., Numerical calculations of critical densities for lines and planes. Journal of Physics A: Mathematical and General, 17(14), pp. 2823–2830, 1984. [22] Charlaix, E., Guyon, E. & Rivier, N., A criterion for percolation threshold in a random array of plates. Solid State Communication, 50(11), pp. 999– 1002, 1984. [23] Wilke, S., Guyon, E. & de Marsily, M., Water penetration through rocks: test of a three-dimensional percolation description. Mathematical Geology, 17(1), pp. 17–24, 1985. [24] Alboin, C., Jaffré, J., Joly, P., Roberts, J.E. & Serres, C., A comparison of methods for calculating the matrix block source term in a double porosity model for contaminant transport. Computational Geosciences, 6, pp. 523– 543, 2002.


211

[25] Brebbia, C.A., Telles, J.C. & Wrobel, L.C., Boundary Elements Techniques, Springer-Verlag: Berlin, 1984. [26] Zagar, I. & Skerget, L., Integral formulations of a diffusive-convective transport equation, BE applications in Fluid Dynamics, eds. C.A. Brebbia & H. Power, Computational Mechanics Publications: Southampton, Boston, pp. 153–176, 1995. [27] Nardini, D. & Brebbia, C.A., A new approach to free vibration analysis using boundary elements. Applied Mathematical Modelling, 7, pp. 157– 162, 1983. [28] Partridge, P.W., Brebbia, C.A. & Wrobel, L.C., The Dual Reciprocity Boundary Elements Method, Computational Mechanics Publications: Southampton, Boston, 1992. [29] Golberg, M.A. & Chen, C.S., The theory of radial basis functions applied to the BEM for inhomogeneous partial differential equations. Boundary Elements Communications, 5, pp. 57–61, 1994. [30] Popov, V. & Power, H., DRM-MD approach for the numerical solution of gas flow in porous media with application to landfill. Engineering Analysis Boundary Elements, 23, pp. 175–188, 1999. [31] Popov, V., Power, H. & Baldasano, J.M., BEM solution of design of trenches in a multi-layered landfill. Journal of Environmental Engineering, 124/1, pp. 59–66, 1998. [32] Popov, V. & Power, H., Numerical analysis of the efficiency of landfill venting trenches. Journal of Environmental Engineering, 126/1, pp. 32–38, 2000. [33] Popov, V. & Power, H., The DRM-MD integral equation method: an efficient approach for the numerical solution of domain dominant problems. International Journal of Numerical Methods in Engineering, 44, pp. 327–353, 1999. [34] Florez, W.F. & Power, H., DRM multidomain mass conservative interpolation approach for the BEM solution of the two-dimensional NavierStokes equations. Computers & Mathematics with Applications, 43(3–5), pp. 457–472, 2002. [35] Florez, W.F. & Power, H., Multi-domain mass conservative dual reciprocity method for the solution of the non-Newtonian Stokes equations. Applied Mathematical Modelling, 26/3, pp. 397–419, 2002. [36] Florez, W.F., Nonlinear Flow Using Dual Reciprocity, WIT Press: Southampton, 2001. [37] Samardzioska, T. & Popov, V., Numerical comparison of the equivalent continuum, non-homogeneous and dual porosity models for flow and transport in fractured porous media. Advances in Water Resources, 28, pp. 235–255, 2005. [38] Natalini, B. & Popov, V., Tests of radial basis functions in the 3D DRM-MD Communications in Numerical Methods in Engineering, 22(1), pp. 13–22, 2005.

212 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES [39] Peratta, A. & Popov, V., A new scheme for numerical modelling of flow and transport processes in 3D fractured porous media. Advances in Water Resources, 29(1), pp. 42–61, 2006. [40] Peratta, A., BEM applied to Flow and Transport in Fractured Porous Media, PhD Thesis, Wessex Institute of Technology, Southampton, UK, University of Wales, December 2004. [41] Saad, Y. SPARSKIT, A Basic Tool Kit for Sparse Matrix Computations. Technical Report RIACS-90-20, Research Institute for Advanced Computer Science, NASA Ames Research Center: Moffett Field, CA, 1990. [42] US EPA, Phase I Comments for Dichlorvos (D238925; Case No. 819293; Chemical No. 084001), Memorandum-Peer review of DDVP, 1999 http://www.epa.gov/oppsrrd1/op/ddvp/efedrisk.pdf [43] Macler, B.A. & Pontius, F.W., Update on the groundwater disinfection rule. Journal of the American Water Works Association, 89(1), pp. 16–20, 1997. [44] WHO, Disinfection of Water, Local Authorities, Health and Environment, Briefing pamphlet series, No. 3 (1995). [45] Simpson, K.J. & Hayes, K.P., Drinking water disinfection by-products: An Australian perspective. Water Research, 32(5), 1522–1528, 1998. [46] Compilation of physical and physico/chemical data of clay materials and steel containers that are suitable for waste isolation, LowRiskDT Project, D2.2 Report, March 2002.

Appendix to Chapter 2 A2.1 Austria A2.1.1 Active mines and mineral production Mines in Austria and their annual production for 1998 are shown in Table A2.1. Table A2.1: Mines in Austria (based on the US Geological Survey).

Mineral Coal Graphite Graphite Graphite Gypsum Gypsum Gypsum Iron ore Magnesite Magnesite

Talc

Tungsten

Operating companies Graz-Koflacher Eisenbahn und Bergbaugesellschaft GmbH (Government 100%) Industrie und Bergbaugesellschaft Pryssok & Co KG Grafitbergbau Kaiserberg Franz Mayr-Melnhof & Co Grafitbergbau Trieben GmbH Erste Salzburger GipswerkGesellschaft Christian Moldan KG Rigips Austria GmbH Knauf Gesellschaft GmbH Voest-Alpine Erzberg GmbH (Government 100%) Veitsch-Radex Radex Austria AG (Osterreichische Magnesit AG 100%) Luzenac Naintsch AG

Wolfram Bergbau und Hόtten GmbH Mittersill

Name of the mines/ location Oberdorf Mine Trandorf Mine at Móhldorf

Annual production (103 tons) 1,200 15

Kaisersberg Mine

3

Trieben Mine Abtenau and Moosegg Mines

3 300

Grundlsee, Puchberg, Unterkainisch, and Weisenbach Mines Hinterstein Mine Erzberg Mine at Eisenerz

250

AG Mines at Breitenau, Hochfilzen and Radenthein Millstatteralpe Mine

Mines at Lassing, Rabenwald, and Weisskirchen, Plants at Oberfeistitz and Weisskirchen Mine, Salzburg; conversion plant, Bergla

160 2,000 600 250 160

350

214 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES A2.1.2 Inactive mines No specific information could be retrieved on inactive mines of the country except Schmitzbe coal mine, which closed in 1995, and Trimmelkam, which closed in 1992. A2.2 Belgium A2.2.1 Active mines and mineral production Mineral production in Belgium for the years 1996–1998 is presented in Table A2.2. Table A2.2: Production of industrial minerals in Belgium (based on the US Geological Survey). Production (103 tons, unless otherwise specified) Mineral Dolomite Limestone Petit granite (Belgian bluestone) (m3) Sodium sulphate

1996

1997

1998

3,379 33,000 1,200,000

3,466 30,000 1,200,000

3,500 30,000 1,000,000

250

250

250

The country has been an important producer of marble for more than 2000 years. All the marble quarries are in Wallonia. Active mines and quarries in Belgium and their annual production for 1998 are shown in Table A2.3. Table A2.3: Active mines and quarries in Belgium (based on the US Geological Survey).

Mineral Dolomite Dolomite Dolomite Limestone

Operating companies SA Dolomeuse (Group Lhoist) SA de Marche-les-Dames (Group Lhoist) SA Dolomies de Merlemont (Group Lhoist) Carmeuse S.A. (Long View Investment NV)

Name of the mines/location Quarry at Marche les Dames Quarries at Namèche Quarry at Philippeville Mines at Engis

Annual production (103 tons) 500 3,000 100 1,850 continued

APPENDIX TO CHAPTER 2

215

Table A2.3: Continued.

Mineral Limestone Limestone Limestone Limestone

Annual production (103 tons)

Name of the mines/location

Operating companies Carmeuse S.A. (Long View Investment NV) Carmeuse S.A. (Long View Investment NV) Carmeuse S.A. (Long View Investment NV) SA Transcar (Royal Volker Stevin)

Mines at Frasnes

450

Mines at Maizeret

850

Mines at Moha

800

Mines at Maizeret

850

A2.2.2 Inactive mines Very little information has been retrieved about inactive mines in Belgium. The only abandoned mines found are some coal mines, located throughout the country. These mines are presented in Table A2.4. Table A2.4: Inactive mines in Belgium. Name

Mineral exploited

Location

Le Hasard (Cheratte) (underground mine) Blegny-Trembleur

Coal

Liége

Coal

Liége

Bas Bois

Coal

Liége

Houthalen Winterslag Andre Dumont

Coal Coal Coal

Eisden Kleine Heide

Coal Coal

Voort Monceau-Fontaine 14

Coal Coal

Kempen Kempen Waterschei (Kempen) Kempen Beeringen (Kempen) Zolder (Kempen) Charleroi

Marcinelle Nord

Coal

Charleroi

Dates of Operation 1860s–1977 Closed until the mid 1980s Closed until the mid 1980s Closed until 1992 Closed until 1992 Closed until 1992 Closed until 1992 Closed until 1992 Closed until 1992 Closed until the mid 1980s Closed until the mid 1980s continued

216 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.4: Continued. Mineral exploited

Location

Dates of Operation

Bois du Cazier

Coal

Charleroi

St Catherine

Coal

Charleroi

Anderlues

Coal

Centre

St Albert in Ressaix

Coal

Centre

Bois du Luc in Houdeng Aimeries

Coal

Centre

Closed until the mid 1980s Closed until the mid 1980s Closed until the mid 1980s Closed until the mid 1980s Closed until the mid 1980s

Name

Note: Due to lack of available information, it is not possible to determine which of the above are underground mines, except ‘Le Hasard’ mine.

A2.3 Denmark A2.3.1 Active mines and mineral production Denmark has no known economically exploitable reserves of metallic ores, so the mining activity is concentrated in industrial minerals. Tables A2.5 and A2.6 show the production of industrial minerals and active mines, respectively. Table A2.5: Production of industrial minerals (based on the US Geological Survey). Production (tons unless otherwise specified) Mineral Chalk Clays (e) Fire clay Kaolin Other Moler, extracted (thousand cubic meters) Lime, hydrated and quicklime Salt, all forms

1996

1997

359,378

427,634

1,800 3,000 8,050

20 (*) 3,000 8,000

185

185

108,628 600,000 (*)

115,129 600,000 (e)

1998 425,000 20 2,500 6,000 185 116,000 600,000 continued


217

Table A2.5: Continued. Production (tons unless otherwise specified) Mineral Sand and gravel (e) Onshore (thousand cubic meters) Offshore (thousand cubic meters) Stone Dimension (mostly granite) (e) Limestone Agricultural Industrial (e)

1996

1997

18,000 5,000

18,000 5,000

18,000 5,000

27,198 (*)

26,000

26,000

695,380 250,000

700,000 (e) 250,000

1996

700,000 250,000

Note: Table includes data available through March 1999 based on estimated sales of domestically produced mineral commodities; * reported production; e, estimated. Table A2.6: Active mines in Denmark (based on the US Geological Survey).

Mineral

Major operating companies and major equity owners

Chalk

A/S Faxe Kalkbrud

Location of main facilities Quarries at Stevns and Sigerslev Quarries on Mors and Fur Islands

Diatomite (moler) Dansk Moler Industri (thousand cubic A/S (Damolin) meters) Kaolin Aalborg Portland A/S Mine and plant on Bornholm Island Salt Dansk Salt I/S Mine (brine) at Hvornum, plant at Mariager

Annual capacity (103 tons) 250 145 25 600

A2.3.2 Inactive mines No specific information could be retrieved on inactive mines of the country.

A2.4 Finland A2.4.1 Active mines and mineral production The ore output of Finnish mines between 1944 and 1999 is shown in Fig. A2.1.


Figure A2.1: Ore output of Finnish mines between 1944 and 1999 (based on the Geological Survey of Finland). The metallic ore mines in Finland for 1998 are shown in Table A2.7. Table A2.7: Metallic ore mines (based on the US Geological Survey).

Mineral Chromite


Outokumpu Oyj (Government, 40%; Insurance Co., 12.3%) Copper: Ore, Outokumpu Oyj Cu content (Government, 40%; Insurance Co., 12.3%) Gold: Ore, Outokumpu Oyj Au content (Government, 40%; (tons) Insurance Co., 12.3%) Gold: Ore, Williams Resources Au content Inc. (tons)

Location of main facilities Mine at Kemi

Mines at Pyhasalmi, Saattopora, and Hitura Mine at Orivesi

Pahtavaara Mine near Sodankyla

Annual capacity (103 tons) Mine type 1,000

OP+UG

10

UG

4

UG

3

OP

continued


219


Mineral


Nickel: Ore, Ni content

Outokumpu Oyj (Government, 40%; Insurance Co., 12.3%) Zinc: Ore, Zn Outokumpu Oyj content (Government, 40%; Insurance Co., 12.3%)

Location of main facilities Mine at Hitura Mine at Pyhasalmi

Annual capacity (103 tons) Mine type 3

UG

25

UG

OP, open-pit; UG, underground mining. In addition, limestone mines and industrial mineral mines according to the Geological Survey of Finland for 1999 are shown in Tables A2.8 and A2.9, respectively. Table A2.8: Limestone mines (based on the Geological Survey of Finland). Mine Parainen Ihalainen Putkinotko Ruokojärvi Ryytimaa Tytyri Förby Siikainen Sipoo Kalkkimaa Ankele Reetinniemi

District

Mineral

Owner

Parainen Lappeenranta Vampula Kerimäki Vimpeli Lohja Särkisalo Siikainen Sipoo Tornio Virtasalmi Paltamo

Lms Lms, Wol Dol Lms, Dol Dol Lms Lms Dol Dol, Lms Dol Dol Dol

Partek Nordkalk Partek Nordkalk Partek Nordkalk Partek Nordkalk Partek Nordkalk Partek Nordkalk Karl Forsström Partek Nordkalk Partek Nordkalk Saxo Minerals Saxo Minerals Juuan Dolomiittikalkki Partek Nordkalk Partek Nordkalk Juuan Dolomiittikalkki Partek Nordkalkk

Vesterbacka Vimpeli Mustio Karjaa Matara Juuka

Lms Lms Dol

Siivikkala

Dol

Total

Vampula

Total ore output (tons)

Mine type

1,279,870 1,172,826 151,834 251,838 184,816 197,367 170,225 91,517 158,670 92,012 72,078 34,820

OP+UG OP OP+UG UG OP UG UG OP UG OP OP OP

22,865 20,819 17,345

OP OP OP

14,216

OP

3,934,785

Lms, limestone; Wol, wollastonite; Dol, dolomite; OP, open-pit; UG, underground mining.

220 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.9: Industrial mineral mines (based on the Geological Survey of Finland).

Mine Siilinjärvi Horsmanaho Lahnaslampi Kinahmi Lipasvaara Kemiö Ristimaa Haapaluoma Total

District

Mineral

Owner

Siilinjärvi Polvijärvi Sotkamo Nilsiä Polvijärvi Kemiö Tornio Peräseinäjoki

Ap, Lms Tlc, Ni Tlc, Ni Qz Tlc, Ni Qz, Fsp Qz Fsp

Kemira Chemicals Mondo Minerals Mondo Minerals SP Minerals Mondo Minerals SP Minerals Saxo Minerals SP Minerals

Total ore output (tons) 8,818,542 491,651 589,441 182,534 58,013 52,570 54,982 0 10,247,733

Mine type OP OP OP OP OP OP OP OP

Ap, apatite; Lms, limestone; Tlc, talc; Fsp, feldspar; Qz, quartz; OP, open-pit. Figure A2.2 shows the location of the major active mines in Finland.

Metallic 1. Pahtavaara: Au 19962. Kemi: Cr 19693. Hitura: Ni, Cu 19704. Pyhäsalmi: Cu, Zn, S 1962 5. Mullikkoräme: Zn, Cu 1 9966. Orivesi: Au 1994Non-metallic 7. Lahnaslampi: Talc, ni 19698. Kinahmi: Quartz 19109. Siilinjärvi: Apatite, limestone, mica 197910. Horsmanaho: Talc, Ni 198011. Ihalainen: Limestone, wollastonite 191012. Sipoo: limestone, dolomite 193913. Förby: limestone 1917 14. Kemiö: Feldspar, quartz 1966 15. Parainen: Limestone 1898-

Figure A2.2: Major active mines in Finland (based on the Geological Survey of Finland).


221

Figure A2.3 shows the active and inactive gold mines and the significant proven and prospective gold deposits in Finland, while the industrial mineral mines and quarries in Finland are shown in Fig. A2.4.

Figure A2.3: Active and abandoned gold mines and proven and prospective gold deposits in Finland (based on the Geological Survey of Finland).


Figure A2.4: Industrial mineral mines and quarries in Finland (based on the Geological Survey of Finland).


223

A2.4.2 Inactive mines Information about inactive mines in Finland are included in the websites of Geological Survey of Finland and Outokumpu Oy, which is the leading company in this country. These inactive mines are shown in Table A2.10. Table A2.10: Inactive underground mines in Finland. Name

Mineral exploited

Enonkoski

Ni–Cu

Vammala*

Ni–Cu

Kotalahti*

Ni–Cu

Aijala* Metsamonttu* Luikonlahti* Vuonos*

Cu–Zn Cu–Zn–Pb Cu–Zn Cu–Zn

Vihanti* Otanmaki* Kivimaa Saattopora Haveri

Fe Au Au Au

Tervola Kittila Viljakkala

Kuurmanpohja* Mullikkorame

Al–Fe Cu–Zn

Joutseno Mullikkorame

Pyhasalmi

Cu–Zn

Location Enonkoski, Savonlinna Vammala

Owner Outokumpu Finnmines Oy Outokumpu Finnmines Oy Outokumpu Finnmines Oy

Orijarvi Orijarvi Malmikaivos Oy Outokumpu Finnmines Oy Outokumpu Oy Rautaruukki Oy none Outokumpu Oy Baltic Minerals Finland Oy Paroc Oy Ab

Dates of operation 1984–1994 1974–1994 1957–1987 1948–1961 1951–1974 1958–1983 1967–1968 1952–1992 1949–1985 1969–? 1988–1995 18th century and 1942–1962 1 year remaining 5 years remaining

*It cannot be specified whether they are open-pit or underground mines due to lack of information

A2.5 France A2.5.1 Active mines and mineral production Active mines in France and their annual production for 1998 are shown in Table A2.11.

224 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.11: Mines in France (based on the US Geological Survey).

Mineral Andalusite

Barite

Barite Coal Coal

Coal Feldspar

Operating companies Denain-Anzin Minéraux Refractaire Ceramique (DAMREC) Barytine de Chaillac

Société Industrielle du Centre Charbonnages de France (CdF), Bassin de Paris Charbonnages de France (CdF), Bassin de Nord-Pas-de-Calais Charbonnages de France (CdF), Bassin de Lorraine Denain-Anzin Minéraux S.A.

Fluorspar

Société Générale de Recherches et d’Exploitation Minière (SOGEREM)

Gold

Société des Mines du Bourneix (Government)

Gold

Mines d’Or de Salsigne (Eltin Co., 51%; Co., 18%; Peter Hambro Plc., 10%) S.A. de Materiel de Construction La Source Compagnie Minière Mines de Potasse d’Alsace S.A. (MDPA)

Gypsum Kaolin Potash, K2O Salt, rock

Compagnie des Salins du Midi et des Salines Varangeville de l’Est

Talc

Talcs de Luzenac S.A. (Rio Tinto Corp., 100%)

Uranium, U3O8

Compagnie Générale des Matières Nucleaires (COGEMA) (Government)

Name of the mines/location Glomel Mine, Brittany Mine and plant at Chaillac, Indre Province Mine at Rossigno, Indre Province Mines and washeries in middle France Mines and washeries in northern France Mines and washeries in eastern France Mine and plant at St. Chély d’Apcher Mines at Le Burc, Montroc le Moulina, and Trebas Mines in the Saint Yrieix la Perche District, Limoges Ranger Mine near Carcassonne Mine at Taverny Kaolin d’Arvor Mine, Quessoy Mines at Amélie, Marie-Louise, and Theodore, in Alsace Mine at SaintNicolas-de-Port Trimons Mine near Ariège, Pyrenees Mines at Limousin, Vendee, and Hérault

Annual production (103 tons) 75

150

100 2,500 1,000

9,500 55 150

4,000 (kg)

3,000 (kg)

1,500 300 10,000

9,000

350,000 1,800


225

A2.5.2 Inactive mines Various inactive mines are presented in Table A2.12. Table A2.12: Inactive mines in France. Name

Mineral exploited

Location

Ensisheim

Coal

Ungersheim

Coal

Rudolphe

Coal

Marie/ Marie-Louise Staffelfelden

Coal Coal

Berrwiller

Coal

Theodore

Coal

Schoenensteinbach

Coal

Amelie

Coal

Max

Coal

Joseph/Else

Coal

La Mure

Coal

Isére

Carmaux

Coal

Tarn

Saint-Bel

Pyrite

Saint-Pierre-laPalud/Rhône

Mines of Mulhouse Terres Rouges

Potash Iron Bauxite

Lorraine Var Province

Owner

Dates of operation

Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de France Charbonnages de Closed in 1997 France Charbonnages de Closed in 1997 France

ARBED S.A. Aluminium Péchiney Société Anonyme des Bauxites et Alumines

Closed in 1998 Closed in 1993


A2.6 Germany A2.6.1 Active mines and mineral production Production of major minerals in Germany is shown in Table A2.13. Table A2.13: Production of major minerals (based on the European Association of Mining Industries). Production (106 unless otherwise specified) Mineral

1996

1997

1998

Coal Lignite Oil Natural gas (billion m3) Potash Rocksalt Gravel and sand Quartz and quartz sand Quartzite Limestone Gypsum Feldspar (103 tons) Pegmatite (103 tons) Kaolin Bentonite (103 tons) Graphite (103 tons) Fluorspar (103 tons) Barytes (103 tons)

47.9 187.2 2.6 20.7 34.6 4.9 402 28 1.2 20.2 2.6 359.7 319 1.8 491.3 2.6 87.6 218

46.5 177 2.8 20.4 35.9 4.1 382 28.1 1.5 21.3 2.5 567.3 635.2 1.8 511 1 58 121

41.3 166.2 2.9 19.9 37.1 n/a 370 n/a n/a n/a n/a n/a n/a n/a n/a n/a 60.9 210

In addition, major mines in Germany for 1998 are listed in Table A2.14. Table A2.14: Major mines (based on the US Geological Survey and Industrial Minerals).

Mineral Bentonite Chalk

Major operating companies and major equity owners Sόd-Chemie AG Kreidewerke Rugen GmbH

Location of main facilities Gammelsdorf, Bavaria Quarries on Rugen Island

Annual capacity (103 tons) 500 500 continued


227


Mineral


Location of main facilities

Four companies, about 27 mines, including Coal, anthracite and bituminous

Gypsum

Kaolin Limestone Lignite

Lignite

Ruhrkohle AG Saarbergwerke AG Preussag Anthrazit GmbH Gebr. Knauf Westdeutsche Gipswerke GmbH Amberger Kaolinwerke GmbH Harz Kalk GmbH Rheinische Braunkohlenwerke AG (Rheinbraun AG) Lausitzer Braunkohle AG (LAUBAG)

Potash

Kali und Salz AG

Salt (rock)

Kali und Salz AG

14 mines in Ruhr region 5 mines in Saar basin Mine at Ibbenburen Mines in Bavaria, Hesse, Saarrland, Lower Saxony Mines at Groppendorf, Hirschau, and Sachsen Quarries at Bad Kosen, Rubelaand, and Kaltes Tal Surface mines in Rhenish mining area: Garzweiler, Bergheim, Inden, and Hambach Surface mines in Lausatian mining area: Janschwalde/ Cottbus-Nord, Welzow-Sud, Nochten/Reichswalde Mines (17) at BergmannssegenHugo, Niedersachen-Riedel, Salzdetfurth, Sigmundshall, Hattorf, Neuhof-Ellers, and Wintershall Mines at Bad Friedrichshall-Kochendorf, Braunschweig-Luneburg, Heilbronn, Riedel, Stetten, and Wesel (Borth)

Annual capacity (103 tons) Total 72,500 (40,000) (14,000) (2,500) 2,000

100 6,000 105,000

50,000

4,000

15,000

A2.6.2 Inactive mines There are a large number of inactive mines located in Germany. Some of them are shown in Tables A2.15–A2.18. It should be specified that there is not much information about their present condition.

228 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.15: Inactive underground metal mines. Name

Location/Description

Rammelsberg Mine Erzbergwerk Grund

Goslar

Bad Grund (Harz/Lower Saxony), Achenbach, Knesebeck, Wiemannsbucht and Meding Shaft Einheit Mine Elbingerode (Harz/Lower Saxony), 2 shafts Bernard-Koenen 2 Near Sangerhausen (Mansfeld/Sangerhausen) Meggen Mine Lennestadt (North Rhine-Westfalia), Sicilia- und Baro Shafts Lüderich mine Near Bergisch Gladbach (North Rhine-Westfalia), Haupt and Franziska Shaft Schafberg Shaft Mechernich/Eifel Türk Shaft Schneeberg (Erzgebirge/Saxony) Ehrenfriedersdorf Erzgebirge/Saxony, Mine 2 shafts Altenberg Mine Erzgebirge/Saxony Damme 2 Damme, (Lower Saxony) Malapertus Wetzlar, (Sieg / Lahn-Dill) Lower Saxony, Sieg / Lahn-Dill, Waldalgesheim (near Bingen), Oberpfalz (Bavaria) (a large number of remaining headgears of former iron mines)

Mineral exploited

Dates of operation

Lead, zinc, copper Lead, zinc

Closed 1989 Closed 1992

Pyrite

Closed 1990

Copper

Closed 1990

Pyrite, lead, Closed 1992 zinc, baryte Lead, zinc

Closed 1978

Lead Silver Tin

Closed 1991

Tin Iron Iron Iron

Closed 1991

Table A2.16: Inactive underground salt and potash mines. Name Mariaglück


Mineral exploited

Dates of operation

Höfer near Celle (Lower Salt and potash Saxony), shafts: Mariaglück, Habighorst

continued


229

Table A2.16: Continued. Name


Hänigsen near Celle/Lerthe (Lower Saxony), shafts: Niedersachsen (potash) and Riedel I (salt) Bergmannssegen- Lerthe (Lower Saxony), Hugo shafts: Hugo, Bergmannsegen Siegfried Giesen near Hildesheim (Lower Saxony), shaft: Siegfried HildesiaDieckholzen near Hildesheim Mathildenhall (Lower Saxony), shafts: Hildesia, NiedersachsenRiedel

Mineral exploited

Dates of operation

Salt and potash

Closed 1997

Potash

Closed 1994

Potash Potash

Mathildenhall Salzdetfurth

Near Hildesheim (Lower Saxony),

Potash

Closed 1992

Shafts I, II, III Glückauf Bleicherode

Sondershausen Südharz (Thüringen), Shafts I, II, IV, V Südharz, Südharz (Thüringen), shafts: Von Velsen I/II,

Potash Potash

Kleinbodungen Sollstedt Bischofferode

Südharz, Südharz (Thüringen), shafts: Sollstedt, Bernterode I/II Südharz, Südharz (Thüringen), shafts: Bischofferode I/II,

Potash Potash

Closed 1993

Neu-Bleicherode Springen

Werra (Thüringen/Hessen), shafts

Potash

Springen I, II/III, IV/V Alexandershall

Werra (Thüringen/Hessen), remaining: Shaft II

Potash

Table A2.17: Inactive underground coal mines. Mineral exploited

Name

Location

Eward/Hugo

Ruhr

Coal

Westfalen

Ruhr

Coal

Gottelborn/ Reden

Saar

Coal

Wehofen

Duisburg

Coal

Owner Deutsche Steinkohle AG Deutsche Steinkohle AG Deutsche Steinkohle AG

Dates of operation Closed 2000 Closed 2000 Closed 2000

continued

230 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.17: Continued. Name

Mineral exploited

Location Saxony

Martin Hoop Colliery

Anna Colliery

Alsdorf (Aachen) Sophia Jacoba Huchelhoven Colliery (Aachen) Bochum, Essen, Dortmund, etc. (a large number of closed collieries)

Owner

Dates of operation

Coal

Closed 1977

Coal

Closed in the 1990s Closed in the 1990s

Coal Coal

Table A2.18: Other inactive underground mines. Name Glasebach Shaft Schönbrunn Cäcilia, Hermine und Erna Grüberg II Kropfmühl Wilhelm and Schenkenbusch

Mineral exploited

Dates of operation

Straßberg, Harz Schönbrunn/Vogtland Closed shafts in Stulln/ Bavaria, Thülen near Brilon, shaft, closed Bavaria, 2 shafts Witterschlick near Bonn

Fluorspar Fluorspar Fluorspar

Closed 1991 Closed 1991

Wirges area near Montabaur

Clay

Location

Calcspar Graphite Clay

Closed 1997 Closed since the 1990s

shafts Richard, Gute Hoffnung, Lindenborn, Anton and Niedersachsen

shafts Melsbach shaft Glückauf and Steiger Shafts

near Koblenz (shaft, closed) Seilitz-Löthain near Meissen/Elbe

A2.7 Greece A2.7.1 Active mines and mineral production Mineral production in Greece for years 1996–1998 is shown in Table A2.19.


231

Table A2.19: Mineral production in Greece (based on the European Association of Mining Industries). Annual production (103 tons) Minerals Alumina Bauxite Bentonite, activated and processed Lignite Magnesite Magnesia, calcined Magnesia, dead burned Nickeliferous ore Perlite PbS concentrate ZnS concentrate

1996

1997

1998

602 2,452 663

584 1,877 735

622 1,823 800

59,738 682 119 57 2,195 599 11.5 13.6

58,939 623 117 86 1,887 696 26.1 32.6

60,400 n/a 104 100 1,800 n/a 30 39

Active mines in Greece and their annual production for 1998 are shown in Table A2.20. Table A2.20: Active mines in Greece (based on the US Geological Survey).

Mineral

Operating companies

Bauxite

Bauxites Parnasse Mining Co. S.A. (EliopoulosKyriakopoulos Group) Eleusis Bauxites Mines, S.A. (ELBAUMIN) (National Bank of Greece) Delphi-Distomon S.A.; Hellenic Bauxites of Distomon S.A.; (Aluminium de Grèce S.A.) Mykobar Mining Co. S.A. (Silver and Baryte Ores Mining Co. S.A.) Silver and Baryte Ores Mining Co. S.A. Mediterranean Bentonite Co. S.A. (Industria Chemica Mineraria S.p.A., Italy)

Bauxite

Bauxite

Bentonite

Bentonite Bentonite

Name of the mines/location Mines at Fokis

Annual production (103 tons) 2,000

Mines near Drama, Itea, and Fthiotis-Fokis Opencast mines at Delphi-Distomon area Mines at Adamas, Milos Island

300

Mines at Adamas, Milos Island Surface mines on Milos Island

500

500

180

20

continued

232 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.20: Continued.

Mineral

Operating companies

Chromite

Financial-Mining-Industrial and Shipping Corp. (FIMISCO) (IRO) Gold, Au in TVX Hellas (TVX Gold Inc., concentrate Canada Gypsum Lava Mining and Quarrying Co. S.A. Gypsum Titan Cement Co. S.A. Lead, mine, TVX Hellas (TVX Gold Inc., Canada) Pb in concentrate Lignite

Public Power Corporation (Government) Lignite Public Power Corporation (Government) Magnesite, Viomagn-Fimisco Ltd. concentrate (Violignit S.A., 65%, Alpha Ventures, 35%)

Magnesite

Grecian Magnesite S.A.

Nickel, ore

General Mining & Metallurgical Co. S.A. (LARCO) (IRO)

Nickel, ore Perlite Perlite Perlite Pozzolan (Santorin earth) Pozzolan Zeolite Zinc, mined, Zn in concentrate

Silver and Baryte Ores Mining Co. S.A. Otavi Minen Hellas S.A. (Otavi Minen AG, Germany) Do. Bouras Co. Lava Mining & Quarrying Co. Ltd. (Heracles General Cement Co. S.A.) Titan Cement Co. S.A. Silver and Baryte Mining Co. S.A. TVX Hellas (TVX Gold Inc., Canada)



Tsingeli Mines and plant near Volos

25

Kassandra Mines, Olympiada Altsi deposit, Crete Island

25 250 280

Kassandra mines (Olympias and Stratoni), northeast Chalkidiki Megalopolis Mine, central Peloponnesus Ptolemais Mine, near Kozani Mines at Gerorema and Kakavos, at Mantoudhi, northern Euboea Island Mine at Yerakini, Chalkidiki Aghios Ioannis Mines near Larymna Mines at Euboea Mines on Kos and Milos Islands Milos Island Kos Island Quarries in Milos

Mine at Pendalofos Kassandra mines (Olympias and Stratoni), northeast Chalkidiki

7,000 28,000 250

200 500 2,500 300 150 50 350

300 100 25


233

The Greek marble industry plays a leading role in the international dimension stone market, as a result of the marble production in almost all areas of the country, its variety of uses and many colours (ash, black, brown, green, pink, red, and multicoloured) (Fig. A2.5).

MARBLE TYPE Alabaster Green Varicoloured Grey-Black Red Whitish to Grey

Figure A2.5: Location of marble deposits in Greece.

PPC is the major producer of lignite, the predominant fuel in electricity generation in Greece. PPC continued exploration in the basins of Amyntaion, Elasson, Florina, Megalopolis, and Ptolemais. PPC had reserves estimated to be 6.8 billion tons from which 4 billion tons was estimated to be economically recoverable by open pit mining. Most PPC lignite is produced from the Ptolemais-Amyntaion basin with lesser amounts from the Megalopolis basin (Fig. A2.6). A2.7.2 Inactive mines Various inactive mines in Greece are presented in Table A2.21.


Figure A2.6: Lignite deposits in Greece. Table A2.21: Inactive mines in Greece. Name

Mineral exploited

Location

Tsagli

Chromite

Eretria

Chromite

Domokos

Koromilies 1

Bauxite

Amfissa

Paliampela

Bauxite

Amfissa

Psorachi

Bauxite

Amfissa

Kokkinochoma Makrilakoma 1 Sideritis

Bauxite Bauxite Bauxite

Amfissa Amfissa Amfissa

Owner

National Bank of Greece Bauxites Parnasse Mining Co. S.A. Bauxites Parnasse Mining Co. S.A. Bauxites Parnasse Mining Co. S.A.

Exploitation type Underground and Open-pit Open-pit Underground and Open-pit Underground and Open-pit Underground and Open-pit Open-pit Open-pit Open-pit continued


235

Table A2.21: Continued. Name

Mineral exploited

Location

Owner

Stifari

Bauxite

Amfissa

Bauxites Parnasse Mining Co. S.A.

Koromilies 2 Koromilies 3 Makrilakoma 2 Zidani

Bauxite Bauxite Bauxite Asbestos

Amfissa Amfissa Amfissa Kozani

Hellenic Mineral Mining Co. S.A.

Exploitation type Open-pit Open-pit Open-pit Open-pit Open-pit

A2.8 Ireland A2.8.1 Active mines and mineral production Table A2.22 shows the mineral production in Ireland for the years 1996–1998. Table A2.22: Mineral production in Ireland (based on the European Association of Mining Industries). Production (103 tons unless otherwise specified) Mineral

1996

1997

1998

Lead (metal in concentrate) Zinc (metal in concentrate) Silver (’000 kg in lead concentrate) Gypsum Alumina Natural gas (billion m3)

45.3 164.5

45 193

35.9 177.2

14.7 422.8 1,233.5 2.74

13.3 477 1,272.8 2.42

10.8 500 1300 1.79

Today, there are only three active mines in Ireland: the Tara Mine, the Galmoy and Lisheen Mine (Table A2.23). Table A2.23: Irish-based metal mines (based on Dhonau N.B.). Name Navan Galmoy Lisheen

Minerals

Dates of operation

Type of mine

Zn, Pb Zn, Pb Zn, Pb

1977 to at least 2010 1997 to at least 2012 1999 to at least 2015

Underground Underground Underground

236 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES A2.8.2 Inactive mines Some inactive mines in Ireland are shown in Table A2.24 while Fig. A2.7 shows the location of both active and inactive mines. Table A2.24: Inactive mines in Ireland (based on Dhonau N.B.). Name

Minerals

Dates of operation

Tynagh

Cu, Zn, Pb, Ag, Ba

Silvermines Gortdrum Avoca

Zn, Pb, Ba Cu, Hg, Ag Cu, Pyrite

1965–1981 1968–1982 1967–1975 1969–1982 (history of mining since 1725)

Type of mine Open-pit & Underground Underground Open-pit Open-pit and Underground

A2.9 Italy A2.9.1 Active mines and mineral production Major mineral production in Italy for the years 1996–1998 is shown in Table A2.25. Table A2.25: Major mineral production (based on the European Association of Mining Industries). Production (tons unless otherwise specified) Minerals Lead (67% Pb) Zinc (55% Zn) Gold Lignite Oil (103 tons) Natural gas (million N m3) Geothermal steam (103 tons) Barytes Bentonite Dolomite Feldspar and aplite (103 tons) Fluorspar Rocksalt (103 tons) Talc

1996

1997

1998

21,000 20,100 0 223,000 5,430 20,200 31,000 80,500 475,000 781,000 2,300 103,000 2,941 136,000

17,600 15,400 0 203,061 5,400 19,500 32,100 26,300 512,900 760,000 2,200 105,800 3,507 141,000

10,100 4,470 1.2 83,700 5,600 19,160 34,200 36,000 592,000 711,370 2,748 107,000 3,354 138,000


237

Figure A2.7: Location of present and past mines in Ireland (based on Minco plc.).

238 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Active mines in Italy are shown in Table A2.26. Table A2.26: Active mines (based on the US Geological Survey and Industrial Minerals).

Mineral Asbestos Barite Barite Barite Barite Bauxite Bentonite Calcium carbonate Feldspar

Feldspar

Major operating companies and major equity owners Amiantifera di Balangero S.p.A. Bariosarda S.p.A (Ente Mineraria Sarda) Edem S.p.A. (Government) Edemsarda S.p.A. (Soc. Imprese Industriali) Mineraria Baritina S.p.A Sardabauxiti S.p.A. (Government) Industria Chimica Carlo Laviosa S.p.A Omya S.p.A. Maffei S.p.A.

Miniera di Fragne S.p.A. Feldspar Sabbie Silicee Fossanova S.P.A. (Sasifo) Gold Gold Mines of Sardinia Ltd. 70%, Government 30% Lead–zinc, Enirisorse S.p.A. ore (Government) Lignite Ente Nazional per l’Energia Electtrica (ENEL)

Location of main facilities Mine at Balangero, near Turin Mines at Barega and Mont ’Ega, Sardinia Mines at Val di Castello, Lucca Mines at Su Benatzu, Sto Stefano, and Peppixeddu, Sardinia Mines at Marigolek, Monte Elto, and Primaluna, near Milan Mine at Olmedo, Sardinia Mines and plant on Sardinia Island, and a plant near Pisa Mine and plant at Carrara, Nocera Surface mines at Pinzolo, Sondalo, and Campiglia Marittima; underground mine at Vipiteno Surface mine at Alagna Valsesia Surface mine at Fossanova Furtei Mine near Cagliaria, Sardinia Mines at Masua, Monteponi, and Sardinia Surface mines at Pietrafitta and Santa Barbara

Annual capacity (103 tons) 100 100 20 20 20 350 250 Over 500 (1994) (200) (300) (60) (30) 1,400 (kg) 60 1,500

continued


239


Mineral



Marble

A number of companies, Quarries in the Carrara and largest of which include: Massa areas Mineraria Marittima Srl Olivine Nuova Cives Srl. Mine and processing at Vidracco, Piemonte Potash ore Industria Sali Underground mines at Otassici e Affini per Corvillo, Pasquasia, Aziono S.p.A. Racalmuto, and San Cataldo, in Sicily Potash ore Sta Italiana Sali Underground mines at Alcalini S.p.A. Casteltermini and (Italkali) Pasquasia, Sicily Pumice Pumex S.p.A. Quarry, Lipari Island, north of Sicily Pumice Europumice Srl Pian di Valle, La Collina, Le Mandarie and S Giovanni delle Contee Pyrite Nuova Solmine S.p.A. Underground mines at Campiano and Niccioleta Salt, rock Sta Italiana Underground mines at Sali Alcalini Petralia, Racalmuto, and S.p.A. (Italkahi) Realmonte, Sicily Salt, rock Solvay S.p.A. Underground mines at Buriano, Pontteginori, and Querceto, Tuscany Talc Luzenac Val Mines at Pinerolo, near Chisone S.p.A. Turin, and at Orani, Sardinia Talc Talco Sardegna S.p.A. Mine at Orani, Sardinia

A2.9.2 Inactive mines Some inactive mines in Italy are presented in Table A2.27.

Annual capacity (103 tons) 2,000 300 1,300

700 600 150 900 4,000 2,000 120 20

240 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.27: Inactive mines in Italy. Name

Mineral exploited

Location

Pyrite Coal Potash Potash Potash

Niccioleta Sardinia Sicily Sicily Sicily

Niccioleta Pasquasia Racalmuto Realmonte

Dates of operation

Owner

Closed 1992 Carbosulcis S.p.A. Standby Standby Standby

A2.10 Luxembourg A2.10.1 Mines and mineral production Mining activity in Luxembourg is very limited and consists of domestic-scale industrial minerals operations. Thus, no specific information could be retrieved on active and inactive mines of the country.

A2.11 Portugal A2.11.1 Active mines and mineral production Major mineral production in Portugal for the years 1997 and 1998 are shown in Table A2.28. Table A2.28: Mineral production in Portugal (based on the European Association of Mining Industries). Production (103 tons) Mineral Uranium (U3O8) Iron/manganese Beryllium Copper conc. (25% Cu) Tin Tungsten Ornamental rock Industrial rock Pegmatites with lithium

1997

1998

20 18,905 3 444,063 6,511 1,791 1,249,446 86,053,493 6,838

22 19,570 na 469,172 5,594 1,436 na na 7,800 continued


241

Table A2.28: Continued. Production (103 tons) Mineral Salt Feldspathic sands Quartz Feldspar Diatomite Pegmatites (mixed quartz and feldspar) Talc

1997

1998

595,997 8,550 9,177 81,597 1,540 6,200

580,209 9,000 9,000 80,000 1,525 6,000

8,236

8,400

In addition, Fig. A2.8 shows the location of active metallic mines for 1998. Information about the major ones is shown in Table A2.29. Table A2.29: Major mines in Portugal (based on the US Geological Survey).

Mineral Copper

Diatomite Feldspar

Major operating companies and major equity owners Sociedade Mineira de Neves-Corvo S.A. (Somincor) (Government, 51%; Rio Tinto Ltd., 49%) Sociedade Anglo-Portugesa de Diatomite Lda. A.J. da Fonseca Lda.

Tin

Somincor (Government, 51%; Rio Tinto Ltd., 49%)

Tungsten

Beralt Tin and Wolfram (Portugal) Ltd. (Avocet Mining Plc. 100%) Empresa Nacional de Uranio S.A. (Government 100%)

Uranium tons

Location of facilities Neves-Corvo Mine near Castro Verde Mines at Obidos and Rolica Seixigal Quarry, Chaves Neves-Corvo Mine near Castro Verde Panasqueira Mine and plant at Barroca Grande Mines at Guargia, plant at Urgeirica

Annual capacity (103 tons) 500

5 10 5 1,600 150


Figure A2.8: Active metallic mines in Portugal (based on the Geological and Mining Institute of Portugal).


243

Portugal’s active industrial mineral mines in 1998 are shown in Fig. A2.9.

Figure A2.9: Active industrial mineral mines (based on the Geological and Mining Institute of Portugal).

244 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES A2.11.2 Inactive mines The location of some of the country’s inactive mines is presented in Fig. A2.10.

Figure A2.10: Inactive mines (based on the Geological and Mining Institute of Portugal).

A2.12 Spain A2.12.1 Active mines and mineral production The mineral production of Spain, from 1996 to 1998, is shown in Table A2.30.


245

Table A2.30: Mineral production in Spain (based on the European Association of Mining Industries). Production (103 tons unless otherwise specified) Mineral Non-metallic minerals Fluorspar (CaF2) Potash (K2O) Salt Quartz Special clays Magnesite (MgO) Sodium sulphate (Na2SO4) Celestite (SrSO4) Washed kaolin Feldspar Calcium carbonate Metallic minerals Iron Pyrite Copper (metal content) Zinc (metal content) Lead Gold (kg) (metal content) Silver (tons) (metal content) Mercury (tons) (metal content) Tin (tons) (metal content) Energy minerals Anthracite Coal Black lignite Brown lignite Oil Natural gas (million m2) Uranium (tons U3O8)

1996

1997

1998

117 680 3,435 1,438 1,042 200 859 115 318 415 1,650

120 639 3,548 1,460 1,460 171 925 95 296 398 1,750

124 585 3,620 1,480 1,480 170 1,001 111 310 430 1,880

1,263 1,042 38.4 145 24 2,763 103 861 2

58 993 38.4 147 23 1,824 66 389 4

52 868 37.2 128 19 3,295 25 672 5

6,440 7,195 4,071 9,585 513 466 346

6,678 7,200 4,115 8,462 380 178 350

6,393 6,004 3,925 9,750 535 112 351

In addition, active mines in Spain and their production for 1997 are shown in Table A2.31.

246 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.31: Active mines in Spain (based on the US Geological Survey and Industrial Minerals).

Mineral Anthracite

Operating companies Antracitas Gaiztarro S.A.

Name of the mines/ location

Mines at Marνa and Paulina Antracitas de Gillon S.A. Mines near Oviedo Antracitas del Bierzo S.A. Mines near Leon Hulleras del Norte S.A. Various mines (Hunosa) and plant Bituminous Hulleras Vasco Santa Lucia Leonesa S.A. Mine, Leon Minas de Figaredo S.A. Mines near Oviedo Nacional de Carbon del Rampa 3 and San Jose Sur (Encasur) Mines, Cordoba Lignite Empresa Nacional de As Pontes Mine, and Electricidad (Endesa) Andorra Mine, La Coruna Barite Minas de Baritina S.A. Mine and plant in (Kali-Chemie of Espiel area, Cordoba Germany, 100%) Mines and plant at Copper Atlantic Copper Arientero, near (Ore, metal Holding, S.A. Santiago de content) (Freeport Compostela, Corta MacMoRan Inc., 65%, Atalay open pit mine. Ercros Group, 35%) Cerro Colorado open pit mine and Alredo underground mine, in Rio Tinto area Copper Navan Resources Ltd. Migolas and Sotiel areas Fluorspar Fluoruros S.A. Opencast mines at San (Bethelhem Steel Lino and Val Negro Corp., 49%) and underground mine at Eduardo, near Carav – all in Asturias Fluoruros S.A. Mines at Veneros Sur (Bethelhem Steel and Corona, Gijσn Corp., 49%) Gold Rio Narcea Belmonte de Miranda, Asturias Gold Mines, Ltd.

Annual production (103 tons) 2,000 2,000 1,000 3,300 2,000 1,000 200 15,000 50 12

30

6 350

200 3,750 kg continued


247


Mineral

Operating companies

Iron ore

Compania Andaluza de Minas S.A. (Mokta, 62%) Altos Hornos de Vizcaya S.A. (U.S. Steel, 25%) Compania Minera Siderugica de Ponferrada S.A. Minera del Andevalo S.A. Sociedad Minera y Metalurgica de Penarroya Espana S.A. (Penarroya, France 90%) Exploracion Minera International Espana S.A. (EXMINESA) Boliden Apirsa SL

Lead ore

Magnesite

Mercury Potash, ore

Magnesitas de Rubian S.A. Magnesitas Navarras S.A. Minas de Almaden y Arrayanes S.A., (Government, 100%) Potasas de Navarra S.A. Iberpotasas S.A.

Pyrite

Union Explosivos Rio Tinto S.A. Compania Espanola de Mines de Tharsis Rio Tinto Minera S.A. Unνon Explosivos (Rio Tinto, 75%; Rio Tinto Zinc, 25%)

Name of the mines/ location


Mine at Alquife, Granada

4,000

Nine mines in Province of Vizcaya Eight mines in Province of Leon

4,000

Opencast mine at Coba, Huelba Opencast mine at Montos de Los Azules, near Union Murcia Underground mine at Rubiales, Lugo

2,000

Opencast mine Los Frailes, near Seville Mines and plant near Sarria, south of Lugo Mine in Eugui, Navarra Mine and smelter at Almaden Mines and plant near Pamplona Underground mine at Suria Mines at Balsareny/ Sallent and Cardona Mines at Tharsis and Zarza, near Seville Mines and plant at Rio Tinto, near Seville

3,000

25

16 48 220 400 70,000 flasks 300 656 2,000 1,300 900

continued

248 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.31: Continued.

Mineral Sepiolite

Uranium, U3O8 Zinc Ore

Operating companies Tolsa S.A. Silicatos-AngloIngleses S.A. Empresa Nacional del Uranio (Enusa), (Government,100%) Asturiana de Zinc S.A. (Azsa) Boliden Apirsa SL Exploracion Minera International Espana S.A. (EXMINESA) Sociedad Minera y Metalurgica de Penarroya-Espana S.A.

Name of the mines/ location Mine and plant at Vicalvaro, near Toledo Mine and plant at Villecas near Madrid Mines and plant near Ciudad Real

Annual production (103 tons) 100 200 Metric tons

Reocin mines and plants near Torrelavega, Santander Opencast mine Los Frailes, near Seville Underground mine at Rubiales, Lugo

500

Mines and plants at Montos de los Azules y Sierra de Lujar, San Agustin

200

125 500

A2.12.2 Inactive mines No specific information could be retrieved on inactive mines of the country, except those presented in Table A2.32.


249

Figure A2.11: Locations of major mining sites and most dangerous tailing ponds in Spain. Key to mines: (1) Los Frailes, (2) Aznalcollar, (3) Tharsis, (4) Sotiel Coronada, (5) Rio Tinto, (6) A Coruρa, (7) Belmonte de Miranda, (8) San Juan de Nieva, (9) Mutiloa, (10) Almonaster La Real, (11) Filon sur, (12) Castuera, (13) Rielves, (14) Morille, (15) Xinzo de Limia, (16) Catoira, (17) So-brado, (18) Toreno, (19) Soto y Amio, (20) Carrocera, (21) Avilιz, (22) Guardo, (23) Muda, (24) Camaleρo, (25) Udias, (26) Suances, (27) Camargo, (28) Maestu, (29) Miranda de Ebro, (30) Valle de Oca, (31) Ibeas de Juarros, (32) Alfaro, (33) Qiarzun, (34) Vilaller, (35) Osor, (36) Bellmunt, (37) Onteniente, (38) Cartegena, (39) Mazar-ron, (40) Cuevad de Almanzora, (41) Nνjar, (42) Almocita, (43) Berja, (44) La Caro-lina, (45) Alcarecejos, (46) Mestanza, (47) Villamayor de Calatrava, (48) Abenojar, (49) Marbella.

250 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.32: Inactive mines in Spain. Name

Mineral exploited Pb-Zn

Troya

Pb-Zn

Fluorspar

Location

Owner

Underground operation at Reocin The Basque Country, Northern Spain

Asturiana de Zinc S.A. (Azsa) Exminesa (Exploración Minera Internacional España S.A.)

Villabona, near Gijon Open pit mine at Seville

Aznalcollar

Pb-Zn

Lieres* Mosquitera* San Vicente* Entrego* San Mames, Cerezal* Olloniego* Barredo* Polio* San Victor* Santa Barbara* Entrago*

Coal Coal Coal Coal Coal

Nalon, Asturias Nalon, Asturias Nalon, Asturias Nalon, Asturias Nalon, Asturias

Coal Coal Coal Coal Coal Coal

Herrera

Coal

Caudal, Asturias Caudal, Asturias Caudal, Asturias Caudal, Asturias Caudal, Asturias Near Oviedo, Asturias Sabero, Asturias

Dates of operation Production is expected to cease in 2003

Closed in 1992 Boliden Apirsa SL

Operation terminated in 1996 Closed in 1999

Closed in the 1990s

*It cannot be specified whether they are open-pit or underground mines due to lack of information.

A2.13 Sweden A2.13.1 Active mines and mineral production Figure A2.12 shows the location of active mines in Sweden and Table A2.33 shows mineral production in Sweden for years 1996–1998.


Name of deposit 1. Kiruna 2. Pahtohavare (RC) 3. Viscaria (RC) 4. Malmberget 5. Aitik 6. Laisvall 7. Kristineberg 8. Kedtrask (IM) 9. Petiknas 10. Renstrom 11. Kankberg (IM) 12. ?kulla Ostra (RC) 13. Langdal (RC) 14. Bjorkdal (RC) 15.Akerberg (IM) 16. Garpenberg 17.Zinkgruvan

Operator LKAB Viscaria AB Viscaria AB Viscaria AB Boliden AB Boliden AB Boliden AB Boliden AB Boliden AB Boliden AB Boliden AB Boliden AB Boliden AB Williams Resources Inc. Boliden AB Boliden AB North Ltd.

Production (10 3 tons/year) 20,000 290 600 12,000 18,000 1,950 560 130 440 174 Cu, Zn, Pb, Au, Ag 113 130 Au, Cu, Ag 229 Cu, Zn, Pb, Au, Ag

Metal Fe Cu, Au Cu Fe Cu, (Au) Pb, (Zn) Cu, Zn, Pb, Au, Ag Zn

Au Au Cu, Zn, Pb Zn, Pb, Ag

251

Type U U U U O U U O U U U O O

1,000

O

160 930 690

U U U

RC, recently closed; IM, intermittently mined; O, open-pit; U, underground.

Figure A2.12: Active mines in Sweden (based on the Geological Survey of Sweden).

252 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Production of Swedish industrial minerals in 1997 is shown in Table A2.34 while major industrial mineral mines are shown in Table A2.35. Table A2.33: Production of minerals in Sweden (based on European Association of Mining Industries). Production (103 tons unless otherwise specified) Mineral Iron ore products Processed sulphide ores Copper concentrate Lead concentrate Zinc concentrate Gold in concentrate (tons)

1996

1997

1998

21,228 24,902 269 136 292 6.1

21,893 23,895 315 146 284 6.7

20,930 24,182 270 155 297 5.9

Table A2.34: Production of Swedish industrial minerals in 1997 (based on Industrial Minerals). Mineral Dolomite, limestone, lime Silica sand, quartz Quartzite Clays Diabase Olivine Feldspar, talc, graphite, etc.

Production (103 tons) 8,000 375 260 200 115 100 80

Table A2.35: Major industrial mineral mines (based on the US Geological Survey and Industrial Minerals). Major operating companies and major equity owners


Feldspar

Berglings Malm & Mineral AB (Omya GmbH)

Feldspar

Forshammar Mineral AB (Cape Minerals AS) Larsbo Kalk AB (Pluess-Staufer AB) Woxna Graphite AB (Tricorona Mineral AB, 100%)

Mines at Beckegruvan, Hojderna, and Limbergsbo Mines at Limberget and Riddarhyttan Mines at Glanshamar and Larsbo Mine and plant at Kringeltjärn, Woxna

Mineral

Feldspar Graphite

Annual capacity (103 tons) 50 30 20 20

continued


253


Mineral


Kyanite

Svenska Kyanite AB (Svenska Mineral, 100%) Limestone Kalproduktion Storugns AB (Nordkalk AB, 100%) Marble (m3) Borghamnsten AB

Location of main facilities Quarry at Halskoberg Mines at Gotland Island Quarry at Askersund

Annual capacity (103 tons) 10 3,000 15,000

A2.13.2 Inactive mines According to the Swedish authorities on underground exploitation, the total number of abandoned mines is 25 in Northern Sweden and 775 in central and Southern Sweden. The location of some inactive underground mines is shown in Fig. A2.13. Additional information about many of them can be found in Table A2.36. Table A2.36: Inactive underground mines in Sweden. Name

Mineral exploited

Stripa

Fe

Viscaria Langdal Pahtohavare Grangesberg Dannemora

Cu Au, Zn, Cu Cu, Au Fe Fe

Lainejaur

Ni

Enasen Luossavaara Fe Tuollavaara Svappavaara Fe Adak Cu Laver Rakkejaur

Location Stripa

12 km North of Mala Gavleborg

Adak

Cu Norrbotten Zn, Au, Ag

Owner

Dates of operation

Stripa Mine Service AB Viscaria AB Boliden AB Viscaria AB

15th century–1977? Recently closed Recently closed Recently closed Closed 1989 13th century–closed 1992 1941–1945

LKAB LKAB LKAB Swedish 1933–1998? Government Boliden AB 1936–1946 Closed 1988 continued

254 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.36: Continued. Mineral exploited

Name Åkerberg

Au

Rävliden Udden Boliden Långsele Långdal

Zn, Cu, Pb, Au Zn, Cu, Pb, Au Au, Cu, Zn, Pb, Ag Zn, Cu, Pb, Au Zn, Pb, Au, Ag

Kedträsk

Zn

Åkulla Östra

Cu, Au, Ag

Falun Stekenjokk Sala

Cu, Zn, Pb, Au Zn, Cu, Pb Pb, Zn, Ag

Location

Owner

Dates of operation 1989–(temporarily closed 1999) Closed 1991 Closed 1990 Closed 1967 Closed 1991 1967–recently closed Intermittently mined 1998 1997–recently closed Closed 1992 Closed 1988 Closed 1962

Other inactive mines with no additional information available are: Northern district: Brännmyra, Rutjebäcken, Näsliden, Holmtjärn, Kimheden, Hornträskviken, Rävliden, Rävlidmyran, Kankberg, Åkulla västra, Åsen, Östra Högkulla. Southern district: Smålands Taberg (iron), Hohults Mangangruva (manganese), Jakobsbergs Mangangruva (manganese), Kleva Nickelgruva (nickel), Ädelfors Guldgruva (gold), Sunnerskogs Koppargruva (copper), Rolfsby Stora Mangangruva (manganese), Gustavs Mangangruva (manganese), Storgruvan, Vretgruvan (manganese), Hedvigs Zink och Blygruva (zinc, lead), De Beschiska Koppargruvan (copper), Börgeltorps zinkgruva (zinc), Skälö Koppargruva (copper), Bjuvs Stenkolsgruva (coal, clay), Onslunda Gruvor (calcium fluoride), Långbans Gruvor (sulpide minerals), Getö Stora Silvergruva (silver), Hällefors Östra Silvergruva (silver), Åmmebergs Zinkgruvor (zinc), Stråssa gruvfält (iron, sulphide minerals?), Ljusnarsbergsfältet (iron, sulphide minerals?), Stripås Koppargruva (copper), Storgruvan (sulphide minerals?), Falu Koppargruva (copper, silver), Sågmyra Koppargruva (copper), Storgruvan i Furboberget (iron?), Garpenbergs Odalfält (iron).


255

Norrbotten: Vi= Viscaria, Li= Liikavaara, Lav= Laver Skellefte Field: Ad= Adak, Ra= Rakkejaur, Å=Åkerberg, Rä= Rävliden, U= Udden, Bo= Boliden, Ls= Långsele, Ld= Långdal Bergslagen: F = Falun, Gr= Grängesberg, Sal= Sala Other areas: Ste= Stekenjokk, E = Enåsen

Figure A2.13: Location of inactive underground mines in Sweden (based on CM Tracing).


A2.14 The Netherlands A2.14.1 Active mines and mineral production The Netherlands has no commercially exploitable reserves of metal ores. The only active mines that exist in the country extract industrial minerals. Active mines in the Netherlands and their annual production for 1998 are shown in Table A2.37. Table A2.37: Mines in the Netherlands (based on the US Geological Survey). Mineral Limestone Salt Salt


Operating companies Ankerpoort NV (Lhoist SA, 100%) Akzo Salt and Basic Chemicals BV Akzo Salt and Basic Chemicals BV


Mines at Maastricht and Winterswijk

600

Mines at Hengelo

2,000

Mines at Delfzijl

2,000

A2.14.2 Inactive mines No specific information could be retrieved on inactive mines of the country.

A2.15 The United Kingdom A2.15.1 Active mines and mineral production Major mineral production in UK for the years 1996–1998 is shown in Table A2.38. Table A2.38: Major mineral production in the UK (based on the European Association of Mining Industries). Production (103 tons unless otherwise specified) Mineral Coal Natural gas (oil equivalent) Crude petroleum (including condensates) Tin/lead/zinc/iron China/ball clay (sales) Other clays and shale

1996

1997

1998

50,196 84,618 130,007

48,495 86,350 128,205

41,276 90,467 132,602

5.1 3,161 12,483

5.2 3,216 11,795

3.2 3,364 12,394 continued


257

Table A2.38: Continued. Production (103 tons unless otherwise specified) Mineral Limestone and dolomite Chalk (GB only) Sandstone Silica sand Sand/gravel (land/marine) Igneous rock Gypsum Rock salt Brine salt Fluorspar Barytes Potash (KCl)

1996

1997

1998

103,119 9,239 17,522 4,861 96,377 50,903 2,000 2,200 4,812 65 93 1,030

105,034 9,550 18,499 4,704 98,383 48,771 2,000 1,800 4,861 64 74 941

106,000 9,500 18,700 4,600 100,000 49,000 2,000 700 4,800 63 68 1,014

In addition, active mines, their owners and annual production for 1998 are shown in Table A2.39. Table A2.39: Active mines (based on the US Geological Survey).

Mineral Aggregate

Major operating companies and major equity owners ARC Ltd. (Hanson Plc., 100%) Foster Yoeman Ltd.

Ball clay

Watts, Blake, Bearne & Co. Plc.

China clay (kaolin)

ECC Group Plc.

Coal

RJB Mining Plc.

Fluorspar Fluorspar

Durham Industrial Minerals Ltd. Laporte Industries Plc.

Gypsum

British Gypsum Ltd.

Location of main facilities 50 quarries in various locations Glensanda quarry at Oban Various operations in northern and southern Devon Mines and plants in Devonshire and Dorsetshire 19 mines in various locations Mines in Weardale Mill at Stoney Middleton, Mines in Derbyshire Mines in Cumbria, Nottinghamshire, and Sussex

Annual capacity (103 tons) 50,000 15,000 500 3,000 40,000 50 70 3,500

continued

258 DISPOSAL OF HAZARDOUS WASTE IN UNDERGROUND MINES Table A2.39: Continued. Major operating companies and major equity owners

Mineral Potash Salt, rock Salt, rock Sand and gravel Silica, sand

Slate, natural Talc Talc

Tin, ore

Cleveland Potash Ltd. Imperial Chemical Industries Plc. Irish Salt Mining and Exploration Co. TMC Pioneer Aggregates Ltd. Hepworth Minerals and Chemicals Ltd. Alfred McAlpine Slate Ltd. Alex Sandison and Son Ltd. Shetland Talc Ltd. (Anglo European Minerals Ltd., 50%; Dalriada Mineral Ventures Ltd. 50%) Crew Group of Canada


Annual capacity (103 tons)

Boulby Mine, Yorkshire 500 Mines at Winsford, 3,000 Cheshire Carrick Fergus, Northern 300 Ireland Chelmsford, Essex 1,000,000 Operations in Cambridgeshire, Cheshire Humberside, and Norfolk Penrhyn quarry, Bethesda, North Wales Unst, Shetland Islands

6,000

Cunningsburg, Shetland Islands

35

South Crofty Mine, Cornwall (Closed March 1998)

25 15

1,800

A2.15.2 Inactive mines Some inactive underground mines in the UK are presented in Table A2.40. Table A2.40: Inactive underground mines in the UK. Name Annesley-Bentinck Silverdale (deep mine) South Crofty Frazers Hush Groverake

Location Near Kirkby, Nottinghamshire Staffordshire Redruth, Cornwall Rookhope/North Pennine Rookhope/North Pennine

Mineral exploited

Dates of operation

Coal

Closed in 2000

Coal Tin Fluorspar

Closed in 1998 Closed in 1998 Closed in 1998–1999

Fluorspar

Closed in 1998–1999

Index

A advection-diffusion....................177 alkaline batteries ..................99, 102 arsenic..............................15, 22, 68 B BEASY ..............115, 118, 143, 151 BEM (boundary element method) .....117, 118, 119, 120, 133, 158, 168, 170, 172, 177, 178, 211, 212 bentonite .....40, 42, 45, 58, 92, 107, 113 bioaccumulation ....................22, 23 boundary conditions ...93, 118, 124, 125, 134, 138, 143, 154, 168, 171, 172, 185 C cadmium ....................15, 22, 29, 30 chemical interaction......80, 88, 102, 107 clay barrier....79, 80, 83, 88, 92, 95, 96, 116 clay microstructure ......................92 columnar model .........................127 construction cost ..........................36 continuum approach ..........159, 162 D Darcy law.........................................163 flow.......................................178 velocity .................................259 dichlorvos ...90, 157, 180, 181, 182, 189, 190, 194, 195, 197, 199, 200, 205, 206, 207, 208 Directive 91/157/EEC .................13

Directive 99/31............................ 16 discrete fracture model ...... 160, 162 dispersion ..... 18, 19, 20, 22, 23, 25, 166, 169, 178, 192, 195, 198, 200, 207, 208 DRM (dual reciprocity method)168, 172, 174, 176, 177, 178, 211 E EDZ (excavation disturbed zone) . 62, 69, 76, 77, 97, 99, 104, 118, 119, 120, 121, 122, 123, 124, 125, 129, 130, 133, 134, 135, 136, 141, 143, 152, 155, 179, 180, 181, 184, 185, 187, 189, 192, 195, 198, 199 environmental monitoring ..... 16, 20 F far-field........................................ 77 flow and transport .................... 212 fly ash .................. 22, 27, 35, 71, 88 fracture intersections 164, 178, 179, 184 fundamental solution ......... 169, 173 G Green integral representation formula ......................... 169, 173 groundwater.. 11, 18, 22, 24, 31, 34, 55, 58, 62, 67, 68, 80, 96, 163, 180, 181, 195, 207, 208, 212 H HDPE geomembrane................... 37 hydration ............. 80, 82, 92, 93, 94

hydraulic conductivity ...61, 62, 65, 67, 69, 70, 76, 77, 79, 80, 81, 82, 83, 84, 92, 95, 97, 108, 110, 162, 189, 192, 200, 207, 208 head......162, 163, 165, 169, 177, 187, 198 I incinerated ash .............................19 Integrated Pollution Prevention and Control ....................................15 L landfills ........16, 19, 36, 37, 42, 110 Laplace equation........................169 limestone.39, 40, 43, 44, 46, 47, 61, 67, 72, 79, 80, 125, 129, 135, 152, 155, 157, 180, 181, 197, 198, 199, 200, 206, 208, 209, 219, 220, 252 LowRiskDT ..34, 90, 102, 180, 190, 212 M matching conditions...................177 mercury...13, 15, 19, 22, 45, 68, 88, 89, 90 mines abandoned 39, 48, 61, 67, 71, 72, 79, 116, 158, 215, 253 reference .......................116, 152 room and pillar...50, 55, 58, 115, 125, 127, 128, 152 underground...18, 33, 34, 35, 37, 40, 42, 43, 48, 49, 50, 59, 88, 157, 180, 196, 206, 216, 223, 230, 250, 253, 258 modelling 18, 69, 73, 74, 75, 79, 92, 96, 103, 115, 116, 117, 118, 122, 125, 135, 151, 157, 158, 159, 161, 163, 199, 210, 212 N near-field......................................77

O operational cost ..................... 17, 34 organochlorines ..................... 24, 29 P permeability...... 116, 159, 160, 161, 199 persistent organic pollutants.. 14, 23 pesticides .... 1, 8, 15, 18, 19, 24, 25, 26, 27, 29, 88, 90, 102, 112 pollutants ............................. 27, 166 porous matrix ... 159, 160, 161, 162, 163, 164, 165, 166, 167, 170, 174 pressure swelling ................ 80, 81, 82, 85 water ................. 82, 95, 104, 113 R reaction term.............................. 175 retardation factor ...... 166, 189, 196, 197, 206, 207 risk assessment 20, 34, 35, 158, 208 rock argillaceous.... 62, 72, 77, 79, 80, 95 crystalline 57, 65, 71, 72, 77, 79, 80, 95, 151, 152, 155, 157, 180, 181, 182, 185, 187, 189, 196, 198, 199, 200, 205, 207, 208, 209 stability ......... 115, 116, 128, 152 stress ................................. 71, 72 S safety aspects..................... 189, 199 source term . 99, 102, 103, 104, 167, 168, 171, 210 specific storativity ..................... 162 stress compressive .......................... 142 distribution... 124, 126, 135, 141, 149 principal. 75, 115, 118, 119, 121, 125, 136, 141, 147, 148

tectonic..........124, 148, 149, 155 submodelling .....120, 130, 150, 154 subzones ....................119, 120, 122 T transport of waste materials.........70 U underground facilities ..................34 underground research laboratories ..........................................50, 65 underground storage ..............16, 17 uniaxial compressive strength ...119

W waste acceptance criteria....... 16, 17 waste management1, 5, 7, 9, 12, 17, 27, 60, 158 water saturation 88, 94, 95, 96, 101, 190, 195, 207 WEEE.................. 11, 12, 13, 18, 27 Z zinc ... 13, 22, 40, 41, 42, 43, 44, 45, 46, 47, 157, 180, 181, 182, 196, 197, 206, 207, 208, 228, 238, 254, 256

Environmental Urban Noise Editor: A. GARCÍA, University of Valencia, Spain A comprehensive overview including all the fundamental aspects required to understand this important field. Amongst the subjects covered are physical assessment and rating of urban noise and effects of noise on health. Series: Advances in Ecological Sciences, Vol 8 ISBN: 1-85312-752-3 2001 240pp £88.00/US$136.00/€132.00

of Ecotoxicological Properties of Hazardous Wastes; Hazardous Waste Management Techniques; Legislation Regarding Environmental Effects of Chemicals; Hazardous Waste Reduction and Recycling Techniques; Biodegradation and Bioremediation; Monitoring of Hazardous Waste Environmental Effects; Laboratory Techniques and Field Validation; Effluent Toxicity, Microbiotests; On-line Toxicity Monitoring; Forensic Toxicology; Genotoxicity/Mutagenicity; Exposure Pathways; Risk Assessment; Biotesting and Environmental Control Strategy; Hot Spots and Accidental Spills. WIT Transactions on Biomedicine and Health Volume 10

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Edited by: A. G. KUNGOLOS, University of Thessaly, Greece, C. A. BREBBIA, Wessex Institute of Technology, UK, C. P. SAMARAS, TEI of West Macedonia, Greece, V. POPOV, Wessex Institute of Technology, UK

Environmental Health Risk II

This book addresses the need for the exchange of scientific information among experts on issues related to environmental toxicology, toxicity assessment and hazardous waste management. Publishing papers from the First International Conference on Environmental Toxicology, the text will be of interest to biologists, environmental engineers, chemists, environmental scientists, microbiologists, medical doctors and all academics, professionals, policy makers and practitioners involved in the wide range of disciplines associated with environmental toxicology and hazardous waste management. The text encompasses themes such as: Acute and Chronic Bioassays; Tests for Endocrine Disruptors and DNA Damage; Interactive Effects of Chemicals; Bioaccumulation of Chemicals; Assessment

Editors: C.A. BREBBIA, Wessex Institute of Technology, UK and D. FAYZIEVA, Academy of Sciences, Uzbekistan The proceedings of the second international conference on this topic, this book contains papers under headings such as: Water Quality Issues; Air Pollution; Accident and Man-Made Risks; Risk Analysis; Analysis of Urban Road Transportation Systems in Emergency Conditions. Series: The Sustainable World, Vol 8 ISBN: 1-85312-983-6 2003 260pp £89.00/US$142.00/€133.50

All prices correct at time of going to press but subject to change. WIT Press books are available through your bookseller or direct from the publisher.

Environmental Health in Central Asia

This book provides information on how environmental conditions in Central Asia have been affected by anthropogenic activity. It also reviews research carried out during the last decades on the impact of the environment on the health of the region’s people. Partial Contents: Air Quality and Population Health in Central Asia; Hydrosphere and Health of Population in the Aral Sea Basin; Influence of Environmental Factors on Development of Non-Communicable Diseases; Environment and Infectious Diseases; Environment and Children’s Health in Central Asia. Series: Advances in Ecological Sciences, Vol 17

engineers this volume evaluates current issues in exposure and epidemiology and highlights future directions and needs. Originally presented at the First International Conference on Environmental Exposure and Health, the papers included cover areas such as: METHODOLOGICAL TOPICS Methods Of Linking Epidemiology, Exposure and Health Risk; Multipathway Exposure Analysis and Epidemiology; Statistical and Numerical Methods. SITE RELATED TOPICS - Work Place and Industrial Exposure; Soil Dust and Particulate Exposure; Water Distribution Systems, Exposure and Epidemiology; Air Pollution Exposure and Epidemiology. DATA COLLECTION TOPICS - Use of Remote Sensing and GIS; Data Mining and Applications in Epidemiology. SPECIAL TOPICS - Exposure Specific to the Developing World; Epidemiology of Mixed Chemical and Microbial Exposure; Effects of Rapid Transportation in Epidemiology; Interaction of Social and Environmental Issues and Health Risk. Series: The Sustainable World Vol 14

ISBN: 1-85312-945-3 2004 £84.00/US$134.00/€126.00

ISBN: 1-84564-029-2 2005 apx 400pp apx £140.00/US$224.00/€210.00

The Present and Future Editor: D. FAYZIEVA, Academy of Sciences, Uzbekistan

284pp

Environmental Exposure and Health Edited by: M. M. ARAL, Georgia Institute of Technology, USA, C. A. BREBBIA, Wessex Institute of Technology, UK, M. L. MASLIA, ATSDR/CDC, USA, T. SINKS, NCEH, USA Current environmental management policies aim to achieve sustainability while improving the health, safety and prosperity of the population. This is an interdisciplinary activity that requires close cooperation between different sciences. Featuring contributions from health specialists, social and physical scientists and

WIT eLibrary Home of the Transactions of the Wessex Institute, the WIT electronic-library provides the international scientific community with immediate and permanent access to individual papers presented at WIT conferences. Visitors to the WIT eLibrary can freely browse and search abstracts of all papers in the collection before progressing to download their full text. Visit the WIT eLibrary at http://library.witpress.com

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Cablebolting in Underground Mines

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Hazardous Laboratory Chemicals Disposal Guide

Hazardous Industrial Waste Treatment

Hazardous Industrial Waste Treatment

Hazardous Waste Handbook

Hazardous Waste Compliance

Basic Hazardous Waste Management

Hazardous Waste Handbook

HAZARDOUS MATERIALS AND WASTE MANAGEMENT

Advances in Hazardous Industrial Waste Treatment

Resources and References.. Hazardous Waste and Hazardous Materials Management

Waste Treatment and Disposal, 2nd Edition

Disposal of Radioactive Waste: Forming a New Approach in Germany

Radioactive Waste Management Considering Timescales in the Post-closure Safety of Geological Disposal of Radioactive Waste

Barrier Systems for Waste Disposal 2nd edition

Hazardous Waste Operations and Emergency Response Manual

Cleaning Up the Environment: Hazardous Waste Technology

Hazardous and radioactive waste treatment technologies handbook

Wireless Communication in Underground Mines: RFID-based Sensor Networking

Advances in Hazardous Industrial Waste Treatment (Advances in Industrial and Hazardous Wastes Treatment)

Sustainable Nuclear Power (Sustainable World)

Review of Chemical Agent Secondary Waste Disposal and Regulatory Requirements

Fluid Waste Disposal (Environmental Science, Engineering and Technology)

The Mines Of Behemoth

Disposal of Neutralent Wastes

Journey To The Underground World

Disposal of Hazardous Waste in Underground Mines (Sustainable World)

Cablebolting in Underground Mines

Waste Treatment and Disposal

Waste treatment and disposal

Waste treatment and disposal

Hazardous Laboratory Chemicals Disposal Guide

Hazardous Industrial Waste Treatment

Hazardous Industrial Waste Treatment

Hazardous Waste Handbook

Hazardous Waste Compliance

Basic Hazardous Waste Management

Hazardous Waste Handbook

HAZARDOUS MATERIALS AND WASTE MANAGEMENT

Advances in Hazardous Industrial Waste Treatment

Resources and References.. Hazardous Waste and Hazardous Materials Management

Waste Treatment and Disposal, 2nd Edition

Disposal of Radioactive Waste: Forming a New Approach in Germany

Radioactive Waste Management Considering Timescales in the Post-closure Safety of Geological Disposal of Radioactive Waste

Barrier Systems for Waste Disposal 2nd edition

Hazardous Waste Operations and Emergency Response Manual

Cleaning Up the Environment: Hazardous Waste Technology

Hazardous and radioactive waste treatment technologies handbook

Wireless Communication in Underground Mines: RFID-based Sensor Networking

Advances in Hazardous Industrial Waste Treatment (Advances in Industrial and Hazardous Wastes Treatment)

Sustainable Nuclear Power (Sustainable World)

Review of Chemical Agent Secondary Waste Disposal and Regulatory Requirements

Fluid Waste Disposal (Environmental Science, Engineering and Technology)

The Mines Of Behemoth

Disposal of Neutralent Wastes

Journey To The Underground World

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